Category: 104-86-9

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. Application In Synthesis of 104-86-9.

Culletta, Giulia;Allegra, Mario;Almerico, Anna Maria;Restivo, Ignazio;Tutone, Marco research published 《 In Silico Design, Synthesis, and Biological Evaluation of Anticancer Arylsulfonamide Endowed with Anti-Telomerase Activity》, the research content is summarized as follows. Telomerase, a reverse transcriptase enzyme involved in DNA synthesis, has a tangible role in tumor progression. Several studies have evidenced telomerase as a promising target for developing cancer therapeutics. The main reason is due to the overexpression of telomerase in cancer cells (85-90%) compared with normal cells where it is almost unexpressed. In this paper, we used a structure-based approach to design potential inhibitors of the telomerase active site. The MYSHAPE (Mol. dYnamics SHared PharmacophorE) approach and docking were used to screen an inhouse library of 126 arylsulfonamide derivatives Promising compounds were synthesized using classical and green methods. Compound 2C revealed an interesting IC₅₀ (33 ± 4 μM) against the K-562 cell line compared with the known telomerase inhibitor BIBR1532 IC₅₀ (208 ± 11 μM) with an SI ∼10 compared to the BALB/3-T3 cell line. A 100 ns MD simulation of 2C in the telomerase active site evidenced Phe494 as the key residue as well as in BIBR1532. Each moiety of compound 2C was involved in key interactions with some residues of the active site: Arg557, Ile550, and Gly553. Compound 2C, as an arylsulfonamide derivative, is an interesting hit compound that deserves further investigation in terms of optimization of its structure to obtain more active telomerase inhibitors.

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., Application In Synthesis of 104-86-9

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). 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. 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 104-86-9.

Dhananjaya, G.;Venkateshwarlu, Rapolu;Dinne, Naresh Kumar Reddy;Kumar, Avula Mahesh;Mekala, Ramamohan;Anna, Venkateswara Rao;Kapavarapu, Ravikumar;Pal, Manojit research published 《 Wang-OSO₃H catalyzed green synthesis of bioactive isoindolo[2,1-a]quinazoline-5,11-dione derivatives: An unexpected observation》, the research content is summarized as follows. The sulfonic acid-functionalized Wang resin (Wang-OSO₃H) was explored as a polymeric and recoverable acidic catalyst for the synthesis of isoindolo[2,1-a]quinazoline-5,11-diones I (R¹ = H, Cl, Br; R² = Me, HCCCH₂, cyclopropyl, 2-MeOC₆H₄, etc.) under green conditions. Thus, the Wang-OSO₃H catalyzed multicomponent reaction (MCR) of an R¹-substituted isatoic anhydride, 2-formylbenzoic acid and various amines R²NH₂ in pure water afforded a range of desired products I in good to excellent (86-94%) yields. The methodol. could be performed under open air and is amenable for scale-up synthesis. The catalyst could be recovered and recycled for several times without significant loss of its catalytic activity. The unexpected formation of 2-(1-hydroxy-3-oxoisoindolin-2-yl)benzamide derivative as observed in one case may allow the access of this class of heterocycles from the same MCR by using an appropriate amine. In silico assessment suggested that the compound I (R¹ = H; R² = 4-MeOC₆H₄CH₂), a known inhibitor of TNF-α, could be a potential ligand for SARS-CoV-2 with which it formed H-bonds through its OMe and two C=O groups.

Related Products 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

Chlorinated organic compounds are found in nearly every class of biomolecules. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. Related Products of 104-86-9.

Cui, Penglei;Li, Sida;Wang, Xianjin;Li, Ming;Wang, Chun;Wu, Lipeng research published 《 Visible-Light-Promoted Unsymmetrical Phosphine Synthesis from Benzylamines》, the research content is summarized as follows. Herein, by applying visible-light photoredox catalysis, the authors have achieved the catalytic deaminative alkylation of diphenylphosphine and Ph phosphine with benzylamine-derived Katritzky salts at room temperature The use of Eosin Y as photoredox catalyst and visible light can largely promote the reaction. Unsym. tertiary phosphines were successfully synthesized, including phosphines with three different substituents that are otherwise difficult to obtain.

Related Products 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

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. Application In Synthesis of 104-86-9.

Culletta, Giulia;Allegra, Mario;Almerico, Anna Maria;Restivo, Ignazio;Tutone, Marco research published 《 In Silico Design, Synthesis, and Biological Evaluation of Anticancer Arylsulfonamide Endowed with Anti-Telomerase Activity》, the research content is summarized as follows. Telomerase, a reverse transcriptase enzyme involved in DNA synthesis, has a tangible role in tumor progression. Several studies have evidenced telomerase as a promising target for developing cancer therapeutics. The main reason is due to the overexpression of telomerase in cancer cells (85-90%) compared with normal cells where it is almost unexpressed. In this paper, we used a structure-based approach to design potential inhibitors of the telomerase active site. The MYSHAPE (Mol. dYnamics SHared PharmacophorE) approach and docking were used to screen an inhouse library of 126 arylsulfonamide derivatives Promising compounds were synthesized using classical and green methods. Compound 2C revealed an interesting IC₅₀ (33 ± 4 μM) against the K-562 cell line compared with the known telomerase inhibitor BIBR1532 IC₅₀ (208 ± 11 μM) with an SI ∼10 compared to the BALB/3-T3 cell line. A 100 ns MD simulation of 2C in the telomerase active site evidenced Phe494 as the key residue as well as in BIBR1532. Each moiety of compound 2C was involved in key interactions with some residues of the active site: Arg557, Ile550, and Gly553. Compound 2C, as an arylsulfonamide derivative, is an interesting hit compound that deserves further investigation in terms of optimization of its structure to obtain more active telomerase inhibitors.

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., Application In Synthesis 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. 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. Related Products of 104-86-9.

Chen, Huiling;Liu, Cheng;Guo, Wei;Wang, Zhiwen;Shi, Yingzhang;Yu, Yan;Wu, Ling research published 《 Functionalized UiO-66(Ce) for photocatalytic organic transformation: the role of active sites modulated by ligand functionalization》, the research content is summarized as follows. In this work, a series of functionalized UiO-66(Ce)-X (X = H, CH₃, Br, NO₂) was successfully synthesized for the photocatalytic oxidation of benzylamines under visible light. The UiO-66(Ce)-CH₃ exhibited the highest conversion among the samples. The quantity and the acid strength of coordinatively unsaturated Ce sites as Lewis acid sites were modulated by ligand functionalization, both following the order of UiO-66(Ce)-CH₃ > UiO-66(Ce)-H > UiO-66(Ce)-Br > UiO-66(Ce)-NO₂, which was closely related to photocatalytic performance. Based on in situ FTIR results, coordinatively unsaturated Ce sites could facilitate the activation of benzylamine mols. via the surface -Ce···N-coordination species, and the activated degree of the N-H bonds was evaluated and compared via the force constant In the photocatalytic process, photogenerated holes achieved the deprotonation of activated benzylamine mols. to form benzylamine cations, and photogenerated electrons captured by oxygen vacancies simultaneously reduced activated O₂ to form O^2-, effectively achieving this selective photooxidation Finally, a synergetic photocatalytic mechanism associated with the coordination activation was proposed to explain this reaction process.

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., Related Products of 104-86-9

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

Chlorinated organic compounds are found in nearly every class of biomolecules. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. Application In Synthesis of 104-86-9.

Chen, Kang;Lv, Shan;Lai, Ruizhi;Yang, Zhongzhen;Hai, Li;Nie, Ruifang;Wu, Yong research published 《 Cobalt-Mediated Decarboxylative/Desilylative C-H Activation/Annulation Reaction: An Efficient Approach to Natural Alkaloids and New Structural Analogues》, the research content is summarized as follows. A Co(II)-mediated decarboxylative/desilylative C-H activation/annulation reaction for the efficient synthesis of 3-arylisoquinolines has been developed [e.g., N-benzylpicolinamide + phenylpropiolic acid → 3-phenylisoquinoline (86%) in presence of Co(OAc)₂ as catalyst, KPF₆ as additive and PEG-400 as solvent; an 80% yield was obtained using 1-phenyl-2-(trimethylsilyl)acetylene instead, under the same optimized conditions.]. Using alkynyl carboxylic acid and alkynyl silane as terminal alkyne precursors provides straightforward routes for the synthesis of natural alkaloids and novel structural analogs.

Application In Synthesis 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

Organic chlorides are organic molecules with a C-Cl bond, for example chloroform (CH3-Cl) or vinyl chloride(C2H3Cl). 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Organic chlorides can be used in production of: PVC, Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. Product Details of C7H8ClN.

Chen, Wenjing;Li, Huafeng;Song, Junpeng;Zhao, Yujie;Ma, Pengtao;Niu, Jingyang;Wang, Jingping research published 《 Binuclear Ru(III)-Containing Polyoxometalate with Efficient Photocatalytic Activity for Oxidative Coupling of Amines to Imines》, the research content is summarized as follows. A novel binuclear ruthenium-based polyoxometalate, K₆H[{Ru₂Cl(H₂O)(CH₃COO)₂}{WO(H₂O)}₂(PW₉O₃₄)₂]·14H₂O (1), was successfully synthesized by the conventional hydrothermal method. Compound 1 was well-characterized by single-crystal X-ray diffraction, X-ray powder diffraction (PXRD), IR (IR) spectroscopy, XPS, electrospray ionization-mass spectrometry (ESI-MS), thermogravimetric analyses (TGA), and elemental anal. The structural unit of compound 1 contains two [A-α-PW₉O₃₄]^9- building blocks at the upper and lower positions connected by two W atoms and two Ru atoms, where the W atoms and Ru atoms are arranged in a trapezoidal arrangement and the Ru atoms are bridged by acetic acid. Furthermore, compound 1 features characteristic absorption bands in the visible region, which allows the investigation of its photocatalytic properties in visible light. Under simulated sunlight radiation (λ > 400 nm), compound 1 exhibits high photocatalytic activity and good circularity toward the oxidative coupling of amines to imines at room temperature with O₂ as the sole oxidant.

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., Product Details of C7H8ClN

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. COA of Formula: C7H8ClN.

Chu, Yunpeng;Wu, Meng;Hu, Fang;Zhou, Panpan;Cao, Zhengqiang;Hui, Xin-Ping research published 《 N-Heterocyclic Carbene-Catalyzed Atroposelective Synthesis of Pyrrolo[3,4-b]pyridines with Configurationally Stable C-N Axial Chirality》, the research content is summarized as follows. The first atroposelective synthesis of pyrrolo[3,4-b]pyridines catalyzed by N-heterocyclic carbene was achieved. A wide range of chiral atropisomers of pyrrolo[3,4-b]pyridines were obtained in high yields with excellent enantioselectivities (96-99% enantiomeric excess). The exptl. results and d. functional theory calculations showed that the C-N axial chirality of the product had high thermal stability.

COA of Formula: 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

Organic chlorides are organic molecules with a C-Cl bond, for example chloroform (CH3-Cl) or vinyl chloride(C2H3Cl). 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Organic chlorides can be used in production of: PVC, Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. Name: (4-Chlorophenyl)methanamine.

Cai, Rongbin;Zhou, Qi;Hou, Tianjiao;Li, Bing;Liu, Yunzhi;Li, Huan;Gao, Yuan;Zhu, Longyi;Luo, Jun research published 《 Facile construction of the all-bridge-position-functionalized 2,4,6,8-tetraazaadamantane skeleton and conversion of its N-functionalities》, the research content is summarized as follows. In this article, an unusual protocol of a “one-pot” three-step strategy to build the special all-bridge-position-functionalized tetraazaadamantane skeletons I [R = i-Bu, Bn, CH₂-2-furyl, etc.] from 2,2-dipropenyl-1,3-dioxolane via ozonation, hydrogenation with 5% Pd/BaSO4, and condensation of the in-situ generated dial intermediate with primary amines was reported for the first time. Different primary amines were compatible with this process and the corresponding 2,4,6,8-tetraalkyl-2,4,6,8-tetraazaadamantane-9,10-dione bis(ethylene ketals) were achieved in 19-46% yields. The conversion of the N-benzyl group to some other functionalities such as acetyl, benzoyl, nitroso and nitro was also investigated.

Name: (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

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.

Cai, Shuai-Fang;Qiu, Li-Qi;Huang, Wen-Bin;Li, Hong-Ru;He, Liang-Nian research published 《 Palladium-catalyzed carboxylative cyclization of propargylic amines with aryl iodides, CO₂ and CO under ambient pressure》, the research content is summarized as follows. A palladium-catalyzed four-component carboxylative cyclization comprising propargylic amines R¹NHCHR²CCR³ (R¹ = Me, Bu, Ph, etc; R² = H, Me, phenyl; R³ = H, Me, Et, pentyl), aryl iodides ArI (Ar = Ph, 2-naphthyl, thiophen-2-yl, etc.), CO₂ and CO was developed. By selecting Et₃N and 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) as the base, resp., both terminal and internal propargylic amines proceeded well facilitated by Pd(PPh₃)₂Cl₂, affording the functionalized 2-oxazolones I in moderate yields. This protocol enlarges the product diversity based on CO₂ conversion and simultaneously provides a cooperative transformation route for both CO₂ and CO.

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