Month: October 2022

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Recommanded Product: (4-Chlorophenyl)methanamine.

Zeng, Le;Wang, Zhonghe;Zhang, Tiexin;Duan, Chunying research published 《 Direct Utilization of Near-Infrared Light for Photooxidation with a Metal-Free Photocatalyst》, the research content is summarized as follows. Near-IR (NIR) light-triggered photoredox catalysis is highly desirable because NIR light occupies almost 50% of solar energy and possesses excellent penetrating power in various media. Herein we utilize a metal-free boron dipyrromethene (BODIPY) derivative as the photocatalyst to achieve NIR light (720 nm LED)-driven oxidation of benzylamine derivatives, sulfides, and aryl boronic acids. Compared to blue light-driven photooxidation using Ru(bpy)₃Cl₂ as a photocatalyst, NIR light-driven photooxidation exhibited solvent independence and superior performance in large-volume (20 mL) reaction, presumably thanks to the neutral structure of a BODIPY photocatalyst and the deeper penetration depth of NIR light. We further demonstrate the application of this metal-free NIR photooxidation to prodrug activation and combination with Cu-catalysis for cross coupling reaction, exhibiting the potential of metal-free NIR photooxidation as a toolbox for organic synthesis and drug development.

Recommanded Product: (4-Chlorophenyl)methanamine, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Product Details of C7H8ClN.

Zeng, Dongwen;Gu, Lijun;Zhang, Lizhu;Li, Ganpeng;He, Yonghui research published 《 Synthesis of aziridines by electrochemical oxidative annulation of chalcones with primary amines》, the research content is summarized as follows. Synthesis of aziridines by electrochem. oxidative annulation of chalcone 1,3-diphenyl-2-propen-1-one with primary amines has been developed under external oxidant – and base-free conditions. The reaction constitutes a new transformation of chalcones with primary amines to aziridines, providing a complementary, simple, and environmentally friendly approach to the currently available methods. A reaction mechanism for this transformation has been proposed based on the cyclic voltammetry.

Product Details of C7H8ClN, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Chloride substituents modify the physical properties of organic compounds in several ways. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. They are typically denser than water due to the presence of chlorine, which has a high atomic weight. Computed Properties of 104-86-9.

Zeng, Dishu;Yang, Tianbao;Tang, Niu;Deng, Wei;Xiang, Jiannan;Yin, Shuang-Feng;Kambe, Nobuaki;Qiu, Renhua research published 《 UV-Light-Induced Dehydrogenative N-Acylation of Amines with 2-Nitrobenzaldehydes To Give 2-Aminobenzamides》, the research content is summarized as follows. Green and efficient method for the synthesis of aminobenzamides ArC(O)NHR [Ar = 2-H₂NPh, 2-H₂N-4-MeC₆H₄, 2-H₂N-4-ClC₆H₄, etc.; R = Ph, Cy, n-Bu, etc.] via UV-light-induced dehydrogenative N-acylation of amines with o-nitrobenzaldehydes was reported. The reaction was also readily achieved on a gram scale. The utility of the 2-aminobenzamide building block in organic synthesis was shown by their use in the preparation of quinazolinone derivatives The method was applied to amino acid derivatives as the amine component, which smoothly gave N-(2-aminobenzoyl)acetate derivatives at room temperature Finally, a plausible mechanism was proposed.

104-86-9, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., Computed Properties of 104-86-9

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Product Details of C7H4Cl2O.

Zaheer, Muhammad;Zia-ur-Rehman, Muhammad;Munir, Rubina;Jamil, Nadia;Ishtiaq, Saiqa;Zaib Saleem, Rahman Shah;Elsegood, Mark R. J. research published 《 (Benzylideneamino)triazole-Thione Derivatives of Flurbiprofen: An Efficient Microwave-Assisted Synthesis and In Vivo Analgesic Potential》, the research content is summarized as follows. Triazole is an imperative heterocycle renowned for its broad-spectrum biol. significance. In this manuscript, facile microwave-assisted synthesis of a series of 4-(benzylideneamino)-3-(1-(2-fluoro-[1,1′-biphenyl]-4-yl)ethyl)-1H-1,2,4-triazole-5(4H)-thione 6(a-m) derivatives along with their in vivo analgesic activity is reported. 2-(2-Fluoro-[1,1′-biphenyl]-4-yl)propanoic acid (flurbiprofen) was converted to Me 2-(2-fluoro-[1,1′-biphenyl]-4-yl)propanoate using microwave irradiation, followed by its hydrazinolysis with hydrazine monohydrate. 2-(2-Fluoro-[1,1′-biphenyl]-4-yl)propanehydrazide thus obtained was converted to 4-amino-3-(1-(2-fluoro-[1,1′-biphenyl]-4-yl)ethyl)-1H-1,2,4-triazole-5(4H)-thione, followed by its condensation with different aromatic aldehydes to get the title compounds Structures of all the synthesized compounds were established using different methods (¹H NMR and ¹³C NMR spectroscopies, mass spectrometry, and elemental anal.) and evaluated for their potential as analgesic agents by tail flick, hot plate, and writhing methods. The results of this in vivo study revealed several compounds as potent analgesic agents among which compound I showed significant analgesic effect for all the three assays employed.

Product Details of C7H4Cl2O, 2,3-Dichlorobenzaldehyde(2,3-DBA)is a useful research compound. Its molecular formula is C7H4Cl2O and its molecular weight is 175.01 g/mol. The purity is usually 95%.
2,3-DBA is an organic compound that is used as a synthetic intermediate in the preparation of other chemicals. It is prepared by reacting 2-chloroacetophenone with hydrochloric acid and sodium carbonate in a reaction vessel. The product can be purified through fractional distillation or crystallization. The optical properties of 2,3-DBA are determined by its dipole moment and the substituents attached to the methylene group. Molecular modeling studies have shown that felodipine can bind to 2,3-DBA through its active methylene group. The reaction products between sulfadiazine and 2,3-DBA are pyridinedicarboxylic acid and 3-chlorobenzaldehyde.
2,3-DBA is part of a group of Benzaldehyde (B119740) derivatives that exhibit activity against Mycobacterium tuberculosis, the bacteria responsible for causing tuberculosis in humans. 2,3-DBA is also used as a reagent to synthesize (E)-2-(2-arylhydrazinyl)quinoxalines, compounds that have potent anticancer activity., 6334-18-5.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

The class of organic compounds having covalently a bonded chlorine atom is called organic chlorides. 6334-18-5, formula is C7H4Cl2O, Name is 2,3-Dichlorobenzaldehyde. Their wide structural variety and divergent chemical properties lead to a broad range of named reactions and applications. Reference of 6334-18-5.

Zaharani, Lia;Ghaffari Khaligh, Nader;Gorjian, Hayede;Rafie Johan, Mohd research published 《 4,4′-trimethylenedipiperidine as a nitrogen heterocycle solvent and/or catalyst: liquid phase tandem Knoevenagel-Michael condensation》, the research content is summarized as follows. Liquid phase tandem Knoevenagel-Michael condensation of various aromatic and heteroaromatic aldehydes with barbituric acid or 2-thiobarbituric acid and malononitrile was studied in a one-pot three-component reaction. For the first time, TMDP was employed as a safe and efficient solvent and/or catalyst in the liquid and aqueous ethanol medium, resp., for the practical and eco-friendly Knoevenagel-Michael condensation. The reactions were carried out by using greener procedures, including (a) the use of TMDP as an N-heterocycle organocatalyst in a green medium including water and ethanol (1:1 volume/volume) at reflux temperature, and (b) the use of TMDP as a dual solvent-catalyst at 65°C in the absence of any solvent. High to excellent yields of the desired pyrano[2,3-d] pyrimidinones were obtained under the two earlier mentioned conditions. The current methodologies have advantages, including (a) avoiding hazardous, toxic, volatile, and flammable materials and solvents, (b) avoiding tedious processes, harsh conditions, and multiple steps for the preparation of catalysts, (c) using a less toxic and noncorrosive catalyst, (d) minimizing hazardous waste generation and simple workup process, and (e) high recyclability of TMDP. Another important result of this work is that the TMDP can be a promising alternative for toxic, volatile, and flammable base reagents such as piperidine and triethylamine in liquid phase organic syntheses owing to its unique properties such as being less toxic, nonflammable, and nonvolatile, and having a low m.p., broad liquid range temperature, high thermal stability, and safe handling and storage.

Reference of 6334-18-5, 2,3-Dichlorobenzaldehyde(2,3-DBA)is a useful research compound. Its molecular formula is C7H4Cl2O and its molecular weight is 175.01 g/mol. The purity is usually 95%.
2,3-DBA is an organic compound that is used as a synthetic intermediate in the preparation of other chemicals. It is prepared by reacting 2-chloroacetophenone with hydrochloric acid and sodium carbonate in a reaction vessel. The product can be purified through fractional distillation or crystallization. The optical properties of 2,3-DBA are determined by its dipole moment and the substituents attached to the methylene group. Molecular modeling studies have shown that felodipine can bind to 2,3-DBA through its active methylene group. The reaction products between sulfadiazine and 2,3-DBA are pyridinedicarboxylic acid and 3-chlorobenzaldehyde.
2,3-DBA is part of a group of Benzaldehyde (B119740) derivatives that exhibit activity against Mycobacterium tuberculosis, the bacteria responsible for causing tuberculosis in humans. 2,3-DBA is also used as a reagent to synthesize (E)-2-(2-arylhydrazinyl)quinoxalines, compounds that have potent anticancer activity., 6334-18-5.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Chlorinated organic compounds are found in nearly every class of biomolecules. 349-88-2, formula is C6H4ClFO2S, Name is 4-Fluorobenzene-1-sulfonyl chloride. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. SDS of cas: 349-88-2.

Zackasee, Jordan L. S.;Al Zubaydi, Samir;Truesdell, Blaise L.;Sevov, Christo S. research published 《 Synergistic Catalyst-Mediator Pairings for Electroreductive Cross-Electrophile Coupling Reactions》, the research content is summarized as follows. A mediator-assisted electrocatalysis is a general strategy for the enhancement of eXEC reactions were demonstrated. While eXEC reactions catalyzed by a variety of widely available ligand-nickel complexes were low yielding when applied to reductive couplings of challenging substrates, reactions with the same complexes generated products in near-quant. yield when a redox-matched mediator was included. A library of catalyst-mediator systems that provided complementary reactivity and enabled coupling of a range of substrate classes in high yields were identified. These catalyst systems were applicable to both chem. and electrochem. reduction, but some required electroreduction due to the low potentials required for activation. Finally, mechanistic studies offered insights that facilitated catalyst-mediator pairing.

SDS of cas: 349-88-2, 4-Fluorobenzenesulfonyl chloride is a useful research compound. Its molecular formula is C6H4ClFO2S and its molecular weight is 194.61 g/mol. The purity is usually 95%.

4-Fluorobenzenesulfonyl Chloride is found to be an excellent activating agent for the covalent attachment of biological substances to a variety of solid supports e.g. Sepharose beads. 4-Fluorobenzenesulfonyl Chloride is also used as a reagent for the studies of proteins by fluorine NMR.

4-Fluorobenzenesulfonyl chloride is a reactive chemical that has been shown to have a low safety profile in humans. It is used in the synthesis of replication inhibitors, which are potential anticancer drugs. It also has been shown to inhibit tumor metastasis and growth in mice by binding to the active site of DNA polymerase and inhibiting DNA replication. 4-Fluorobenzenesulfonyl chloride is stable in human liver cells and has been shown to be an effective macroinitiator for proton-coupled electron transfer reactions. This compound has been shown to induce locomotor activity and energy efficiency in rats, which may be due to its ability to increase the number of mitochondria per cell., 349-88-2.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

The class of organic compounds having covalently a bonded chlorine atom is called organic chlorides. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Their wide structural variety and divergent chemical properties lead to a broad range of named reactions and applications. Computed Properties of 104-86-9.

Yusuf, Mohammad;Hira, Shamim Ahmed;Park, Kang Hyun research published 《 Light-Harvesting Novel Hierarchical Porous Cu₉S₅-MnWO₄ Hybrid Structures in Photocatalytic Oxidative Homocoupling of Alkynes and Amines》, the research content is summarized as follows. The discovery of light-harvesting materials for use in photocatalytic organic reactions has recently attracted attention, indicating the potential for utilizing renewable energy sources. A hybrid semiconductor (SC)-SC structure, Cu₉S₅-MnWO₄, was synthesized using a simple, efficient method. The novel hierarchical porous Cu₉S₅-MnWO₄ hybrid structures were then applied in the photocatalysis of oxidative homocoupling of alkynes and amines. The design of a heterogeneous catalyst based on a porous, SC-SC hybrid structure and low-cost Cu should generate interest in the fabrication and modification of photocatalysts for a wide range of applications.

Computed Properties of 104-86-9, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Chloride substituents modify the physical properties of organic compounds in several ways. 3900-89-8, formula is C6H6BClO2, Name is (2-Chlorophenyl)boronic acid. They are typically denser than water due to the presence of chlorine, which has a high atomic weight. SDS of cas: 3900-89-8.

Yusoff, Hanis Mohd;Bala Chandran, Prasana Devi;Sayuti, Fatin Amira Binti;Kan, Su-Yin;Mohd Radzi, Siti Aisha;Yong, Fu-Siong Julius;Lee, Oon Jew;Chia, Poh Wai research published 《 Highly efficient, recyclable and alternative method of synthesizing phenols from phenylboronic acids using non-endangered metal: Samarium oxide》, the research content is summarized as follows. Oxidation of phenylboronic acid to phenol is one of the important industrial processes and it is generally employed in the plastic, explosive and drug manufacturing industries. Over the past decades, numerous efficient methods have been described for the generation of phenols from phenylboronic acids in the presence of oxidant. However, these methods suffered from various limitations, including the use of expensive, toxic reagents and sophisticated protocol to synthesize the phenols. Addnl., some of these reported literatures employed endangered metals, in which mankind is facing the risk of limited supply of these elements in 20 years’ time from now. As such, a viable alternative and green method for achieving organic synthesis is highly sought after by the chemists of today. Herein, we report for the first time a facile, efficient and alternative method in the preparation of phenols from phenylboronic acids using non-endangered metal as catalyst. In all cases, all phenols were afforded in satisfactory yields (81-96%) by employing column-free method. In the recyclability study, the Sm₂O₃ catalyst was found to possess good catalytic performance, even after being reused for five consecutive times (96-91%). In addition, SEM result revealed that the morphol. of the recycled Sm₂O₃ catalyst was well preserved after five successive uses, which indicate no observable changes occurred in the recovered catalysts. As a final note, the current method is anticipated to be useful for industries manufacturing chem. intermediates as it provides an alternative method of catalysis by using a non-endangered metal in organic transformations.

3900-89-8, 2-Chlorophenylboronic acid is a useful research compound. Its molecular formula is C6H6BClO2 and its molecular weight is 156.38 g/mol. The purity is usually 95%.
2-Chlorophenylboronic acid used in the preparation of imidazo[1,2-a]pyridine amides which has tuberculostatic activity.
2-Chlorophenylboronic acid is a diphenyl ether that can be used as a building block for the synthesis of benzodiazepine receptor ligands. It has been shown to be an efficient nucleophile, leading to the formation of carbonyl groups in the presence of halides. 2-Chlorophenylboronic acid has also been shown to inhibit p38 kinase activity and may be useful for anticancer therapy., SDS of cas: 3900-89-8

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Organic chlorides are organic molecules with a C-Cl bond, for example chloroform (CH3-Cl) or vinyl chloride(C2H3Cl). 12112-67-3, formula is C16H24Cl2Ir2, Name is Chloro(1,5-cyclooctadiene)iridium(I) dimer. Organic chlorides can be used in production of: PVC, Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. Safety of Chloro(1,5-cyclooctadiene)iridium(I) dimer.

Yun, Bo-Sun;Kim, So-Yoen;Kim, Jin-Hyoung;Choi, Sunghan;Lee, Sanghun;Son, Ho-Jin;Kang, Sang Ook research published 《 Synthesis and Characterization of Blue Phosphorescent NHC-Ir(III) Complexes with Annulated Heterocyclic 1,2,4-Triazolophenanthridine Derivatives for Highly Efficient PhOLEDs》, the research content is summarized as follows. Efficient tris-bidentate Ir(III) phosphorescent dopants were prepared using 1,2,4-triazolo[4,3-f]phenanthridine (tzp) moieties modified with aryl substituents (Ph, tolyl, and xylenyl) as the main phenylimidazole-based N-heterocyclic carbene (NHC) chelates (CĈ:). According to the degree of the bulkiness of the aryl substituent and the ligation mode, the five prepared Ir(^tzpCĈ:) complexes include four homoleptic NHC-Ir(III) complexes that are referred to as fac-Ir(tzpPh)₃, fac/mer-Ir(tzpTol)₃, and mer-Ir(tzpXyl)₃ and one heteroleptic cis-Ir(tzpPh)₂(tzpPh)’, in which the Ph moiety of one tzpPh ligand is abnormally ligated to the Ir metal center, unlike other tzp ligands. The Ir(III) complexes ligated by carbene ligands (^tzpCĈ:) exhibited highly efficient emissions in solid state (Φ_em = 23.2-54.0%). Electrochem. and theor. studies revealed that the excited-state properties of these NHC-Ir(III) complexes are variable on the extent of planarity and π-conjugation of the ^tzpCĈ: chelating ligand. Due to its enhanced rigidity and low excited-state energy, a result of abnormal tzpPh ligand ligation, the heteroleptic cis-Ir(tzpPh)₂(tzpPh)’ exhibited the most efficient emission properties in solution (Φ_em = 21.3%) and solid (Φ_em = 54.0%) media. Of the devices fabricated with Ir(^tzpCĈ:)₃ complexes as emitters, that doped with cis-Ir(tzpPh)₂(tzpPh)’ exhibited superior electroluminescence efficiencies (external quantum efficiency (EQE) of 16.3%, current efficiency of 27.6 cd A^-1, and power efficiency of 22.1 lm W^1-) and CIE coordinates of [0.17,0.26], which are superior to those of other Ir(^tzpCĈ:)₃ complexes and Ir(dmp)₃ (dmp = 3-(2,6-dimethyl-phenyl)-7-methylimidazo[1,2-f]phenanthridine). This study provides insight into the mol.-level engineering of Ir(III) dopant materials for improving the emission efficiencies of phosphorescent OLEDs.

Safety of Chloro(1,5-cyclooctadiene)iridium(I) dimer, Bis(1,5-cyclooctadiene)diiridium(I) is a useful research compound. Its molecular formula is C16H24Cl2Ir2-2 and its molecular weight is 671.7 g/mol. The purity is usually 95%.
Bis(1,5-cyclooctadiene)diiridium(I) Dichloride is a catalyst used in the iridium-catalyzed asymmetry hydrogenation of unfunctionalized exocyclic double carbon bonds. Also, it is used to test new NeoPHOX ligands derived from serine or threonine.
Bis(1,5-cyclooctadiene)diiridium(I) dichloride is an acid that can be prepared using a preparative method. It is an organometallic compound that can be used in the cross-coupling of activated terminal alkynes with aryl halides. Bis(1,5-cyclooctadiene)diiridium(I) dichloride has been synthesized by reacting furfural with chloride and acetonitrile. The ligand used was 2,2′-bipyridine. The reaction time to produce bis(1,5-cyclooctadiene)diiridium(I) dichloride is approximately three hours.
, 12112-67-3.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Organic chlorides are organic molecules with a C-Cl bond, for example chloroform (CH3-Cl) or vinyl chloride(C2H3Cl). 3900-89-8, formula is C6H6BClO2, Name is (2-Chlorophenyl)boronic acid. Organic chlorides can be used in production of: PVC, Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. Related Products of 3900-89-8.

Yue, Fuyang;Liu, Jianhua;Ma, Henan;Liu, Yuxiu;Dong, Jianyang;Wang, Qingmin research published 《 Light-Mediated Defluorosilylation of α-Trifluoromethyl Arylalkenes through Hydrogen Atom Transfer》, the research content is summarized as follows. Herein, the authors report a direct, light-mediated defluorosilylation protocol for converting α-trifluoromethyl arylalkenes and alkyl silanes into γ,γ-difluoroallylic compounds via a combination of photoredox catalysis and H atom transfer. The clean, convenient protocol can be scaled to the gram level, and its mild conditions make it very suitable for late-stage functionalization of complex natural products and drugs.

Related Products of 3900-89-8, 2-Chlorophenylboronic acid is a useful research compound. Its molecular formula is C6H6BClO2 and its molecular weight is 156.38 g/mol. The purity is usually 95%.
2-Chlorophenylboronic acid used in the preparation of imidazo[1,2-a]pyridine amides which has tuberculostatic activity.
2-Chlorophenylboronic acid is a diphenyl ether that can be used as a building block for the synthesis of benzodiazepine receptor ligands. It has been shown to be an efficient nucleophile, leading to the formation of carbonyl groups in the presence of halides. 2-Chlorophenylboronic acid has also been shown to inhibit p38 kinase activity and may be useful for anticancer therapy., 3900-89-8.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics