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. Application of C7H8ClN.
Hu, Qizhi;Jiang, Shi;Wu, Yue;Xu, Hongzhong;Li, Guoqing;Zhou, Yu;Wang, Jun research published ã?Ambient-Temperature Reductive Amination of 5-Hydroxymethylfurfural Over Al2O3-Supported Carbon-Doped Nickel Catalystã? the research content is summarized as follows. An efficient catalytic system for the conversion of 5-hydroxymethylfurfural (HMF) into N-containing compounds over low-cost non-noble-metal catalysts is preferable, but it is challenging to reach high conversion and selectivity under mild conditions. Herein, an Al2O3-supported carbon-doped Ni catalyst was obtained via the direct pyrolysis-reduction of a mixture of Ni3(BTC)2·12H2O and Al2O3, generating stable Ni(0) species due to the presence of carbon residue. A high yield of 96% was observed in the reductive amination of HMF into 5-hydroxymethyl furfurylamine (HMFA) with ammonia and hydrogen at ambient temperature The catalyst was recyclable and could be applied to the ambient-temperature synthesis of HMF-based secondary/tertiary amines and other biomass-derived amines from the carbonyl compounds The significant performance was attributable to the synergistic effect of Ni(0) species and acidic property of the support Al2O3, which promoted the selective ammonolysis of the imine intermediate while inhibiting the potential side reaction of over-hydrogenation.
Application 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