Category: 95-88-5

Catalyst and Sensitizer-Free Visible-Light-Induced C(sp²)-H Chalcogenation of Arenes/Heteroarenes with Dichalcogenides was written by Kumaraswamy, Gullapalli;Ramesh, Vankudoth;Gangadhar, Maram;Vijaykumar, Swargam. And the article was included in Asian Journal of Organic Chemistry in 2018.Application In Synthesis of 4-Chlororesorcinol The following contents are mentioned in the article:

A direct selenation of arenes and heteroarenes at room temperature has been accomplished. This protocol was enabled by a visible-light-promoted single-electron-transfer (SET) pathway without a directing group. An array of arenes and heteroarenes, such as indoles, pyrroles, and functionalized aryl substrates could go through this selenation with high yields and regioselectivity. The salient feature of this protocol is the SET achieved by irradiating one of two organic mols. thereby avoiding a sensitizer to form a radical ion pair. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Application In Synthesis of 4-Chlororesorcinol).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Application In Synthesis of 4-Chlororesorcinol

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

Organic Base-Mediated Carboxylation of (Hetero)aromatic Compounds Using Supercritical Carbon Dioxide (scCO₂) was written by Chetty, Lloyd C.;Kruger, Hendrik G.;Arvidsson, Per I.;Naicker, Tricia;Govender, Thavendran. And the article was included in Synthesis in 2022.Computed Properties of C6H5ClO2 The following contents are mentioned in the article:

A straightforward site-selective method for the direct carboxylation of resorcinols (3-hydroxyphenol derivatives), phenols ROH (R = Ph, 3-hydroxyphenyl, 2-methyl-3-hydroxyphenyl, etc.), and indoles I (R¹ = H, Br, nitro) is reported. The products were obtained in moderate to high yields using supercritical carbon dioxide as an electrophile and solvent under basic conditions. This method offers solvent and metal free conditions without the cumbersome exclusion of air or water with convenient purification This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Computed Properties of C6H5ClO2).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Computed Properties of C6H5ClO2

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

Practical regioselective halogenation of vinylogous esters: synthesis of differentiated mono-haloresorcinols and polyhalogenated resorcinols was written by Chen, Xiaohong;Liu, Xiaoguang;Martinez, Jenny S.;Mohr, Justin T.. And the article was included in Tetrahedron in 2016.Safety of 4-Chlororesorcinol The following contents are mentioned in the article:

A practical and efficient method for the direct, regioselective conversion of vinylogous esters to haloresorcinols is reported. Control of the reaction conditions enables synthesis of either the 4- or 6-haloresorcinol isomers from a common precursor with excellent regiocontrol and high yield. The generality and functional group tolerance of this novel protocol is demonstrated. The utility of this methodol. to access polyhaloresorcinols is also reported. These methods create useful functionalized building blocks for further synthetic applications. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Safety of 4-Chlororesorcinol).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.Safety of 4-Chlororesorcinol

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

Synthesis, characterization and antibacterial activities of newly synthesized coumarin derivatives was written by Chavhan, J. V.;Patil, S. S.. And the article was included in International Journal of Pharmaceutical, Chemical and Biological Sciences in 2017.Reference of 95-88-5 The following contents are mentioned in the article:

In this work, substituted coumarin based flavones I (R = OCH₃, NO₂) have been synthesized via chalcone. The study was conducted with two primary objectives. The first objective was to synthesize coumarin based flavones and second objective was to study antimicrobial activity of synthesized compounds The structures of the compounds were elucidated by elemental and spectral (IR, 1HNMR, and MS) anal. The reactions are easy to conduct, under mild conditions, and form coumarine substituted flavones in moderate to excellent yields. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Reference of 95-88-5).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Reference of 95-88-5

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

Synthesis of 2-(pyrrolidin-1-yl)pyrimidines by reactions of N-(4,4-diethoxybutyl)pyrimidin-2-amine with (hetero)aromatic C-nucleophiles was written by Smolobochkin, Andrey V.;Rizbayeva, Tanzilya S.;Gazizov, Almir S.;Voronina, Julia K.;Chugunova, Elena A.;Akylbekov, Nurgali I.;Appazov, Nurbol O.;Burilov, Alexander R.;Pudovik, Michael A.. And the article was included in Chemistry of Heterocyclic Compounds in 2019.Application of 95-88-5 The following contents are mentioned in the article:

A method was developed for the synthesis of 2-(pyrrolidin-1-yl)pyrimidines I•CF₃CO₂H [R = 2,4-di-OH-5-ClC₆H₂, 2-hydroxy-1-naphthyl, 6-hydroxy-1,3-benzodioxol-5-yl, etc.] and 2-[(4,4-diarylbutyl)amino]pyrimidine by reactions of (hetero)aromatic C-nucleophiles with N-(4,4-diethoxybutyl)pyrimidin-2-amine in the presence of trifluoroacetic acid. The structures of the obtained products were confirmed by methods of IR spectroscopy, ¹H and ¹³C NMR spectroscopy and X-ray structural anal. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Application of 95-88-5).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Application of 95-88-5

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

Synthesis and anticancer activity of open-resorcinarene conjugates was written by Daniel Pedro-Hernandez, Luis;Hernandez-Montalban, Carlos;Martinez-Klimova, Elena;Ramirez-Apan, Teresa;Martinez-Garcia, Marcos. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2020.Category: chlorides-buliding-blocks The following contents are mentioned in the article:

The first example of conjugation of open-resorcinarenes with chlorambucil, ibuprofen, naproxen and indomethacin are presented. The cytotoxic properties of the obtained conjugates were tested against the cancer cell lines U-251, PC-3, K-562, HCT-15, MCF-7 and SKLU-1. It was found that the conjugate with chlorambucil, naproxen or indomethacin (having 8 moieties) was toxic towards cancer cell lines U-251 and K-562, with no activity against non-cancerous COS-7 cells. The conjugates with naproxen and indomethacin showed high selectivity towards U-251 tumor cells. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Category: chlorides-buliding-blocks).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Category: chlorides-buliding-blocks

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

Ti(IV) doping: An effective strategy to boost Lewis acidic performance of ZnO catalyst in fluorescein dye synthesis was written by Jadhav, Nirajkumar H.;Shinde, Dnyaneshwar R.;Sakate, Sachin S.;Rasal, Nishant K.;Pawar, Ramdas A.. And the article was included in Catalysis Communications in 2019.Computed Properties of C6H5ClO2 The following contents are mentioned in the article:

Zn_1-xTi_xO NPs were efficiently synthesized using a simple solution free mechanochem. method. The synthesized ZnO and Ti(IV)-doped ZnO catalysts are exhibited polycrystallinity, a hexagonal crystal structure, and roughly spherical agglomerates. The surface areas of the Zn_1-xTi_xO catalysts were pos. correlated with the doping percentage of Ti(IV), which also enhanced the Lewis acidity of the NPs. The catalysts exhibited excellent activity during the synthesis of fluorescein dyes. This methodol. was also extended to sulfone-fluorescein dye synthesis. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Computed Properties of C6H5ClO2).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.Computed Properties of C6H5ClO2

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

New visible light excitable donor-acceptor 7-hydroxy-coumarins as blue fluorescent probes for selective staining of vacuoles in yeasts and L. donovani was written by Raghuvanshi, Ashutosh;Kumar Jha, Ajay;Kathuria, Manoj;Priya Awasthi, Bhanu;Purohit, Deepak;Mitra, Kalyan;Goel, Atul. And the article was included in Journal of Materials Chemistry B in 2017.Application of 95-88-5 The following contents are mentioned in the article:

In order to address the existing limitations of the com. available fluorescent probe CMAC (7-amino-4-chloromethylcoumarin), a new series of highly fluorescent donor-acceptor 7-hydroxy-coumarin derivatives was prepared and these derivatives were used as vacuole specific fluorescent probes for live cell imaging of unicellular parasitic protozoa L. donovani promastigotes and yeast cells S. pombe and S. cerevisiae. The synthesized 7-hydroxy-coumarins exhibited interesting photophys. properties and have advantages such as excitation in the visible region, good water solubility, photo-stability, good quantum yield and low cytotoxicity. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Application of 95-88-5).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Application of 95-88-5

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

Synthesis of 2-Arylpyrrolidines by Reactions of 3-Arylidene-1-pyrrolines with Phenols was written by Smolobochkin, A. V.;Melyashova, A. S.;Gazizov, A. S.;Burilov, A. R.;Pudovik, M. A.. And the article was included in Russian Journal of General Chemistry in 2018.Computed Properties of C6H5ClO2 The following contents are mentioned in the article:

The reaction of 3-arylidene-1-pyrrolines with phenols yielded 2-arylpyrrolidines. The proposed method makes it possible to obtain pyrrolidines containing a phenol fragment in the position 2 in high yields and under mild conditions. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Computed Properties of C6H5ClO2).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Computed Properties of C6H5ClO2

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

Synthesis of 1-(hydroxyaryl)furo[3,4-c]pyridines from 1-amino(alkoxy)furo[3,4-c]pyridines and (poly)phenols was written by Kibardina, Lyudmila K.;Trifonov, Alexey V.;Dobrynin, Alexey B.;Pudovik, Mikhail A.;Burilov, Alexander R.. And the article was included in Mendeleev Communications in 2018.COA of Formula: C6H5ClO2 The following contents are mentioned in the article:

The herein obtained 1-diethylamino-6-methyl-1,3-dihydrofuro[3,4-c]pyridin-7-ol or its 1-ethoxy analog in their reactions with phenols or polyphenols undergo replacement of Et₂N/OEt groups with (poly)hydroxyaryl moieties. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5COA of Formula: C6H5ClO2).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.COA of Formula: C6H5ClO2

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