He, Yujie team published research in ACS Omega in 2022 | 104-86-9

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.

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.

He, Yujie;Zhang, Haipeng;Wang, Zeyan;Zheng, Zhaoke;Wang, Peng;Liu, Yuanyuan;Cheng, Hefeng;Zhang, Xiaoyang;Da, Ying;Huang, Baibiao research published 《 Photoelectrochemical oxidation of amines to imines and production of hydrogen through Mo-doped BiVO4 photoanode》, the research content is summarized as follows. Imines are important multifunctional intermediates for the synthesis of pesticides, pharmaceuticals, biologics, and fine chems. The direct photoelectrochem. (PEC) oxidation of amines to imines is a highly selective, efficient, green, and gentle method. Interestingly, the constructive merging of the PEC oxidation of amines with the production of hydrogen can accelerate hydrogen evolution due to the less challenging oxidation of amines such as benzylamine (BN) in comparison to sluggish water oxidation Herein, Mo-doped BiVO4 photoanodes were prepared and first applied to simultaneously oxide benzylamine (BN) to N-benzylidenebenzylamine (BI) and produce hydrogen in a closed two-chamber, three-electrode PEC cell After illumination at a bias of 1.3 V vs SCE for 3 h, the 3% Mo-doped BiVO4 photoanode achieved a maximum yield of ~94μmol h-1 at a 1 x 1 cm2 area with a BN to BI selectivity of almost 100% and a Faradaic efficiency of 98.4%. Our electrode presented enhanced photocorrosion resistance in acetonitrile solvent. Addnl., the PEC oxidations of benzylamine derivatives with different substituents (-F, -Cl, -Br, -CH3, -OCH3) to the corresponding imines were also investigated. The results indicated that the Mo-doped BiVO4 photoanode exhibited an excellent performance in the oxidation of these benzylamine derivatives with corresponding amine to imine selectivities of almost 100% and Faradaic efficiencies of >95%.

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