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. SDS of cas: 104-86-9.
Ling, Johanne;Bruneau-Voisine, Antoine;Journot, Guillaume;Evano, Gwilherm research published 《 Copper-Catalyzed Carbonylative Cross-Coupling of Alkyl Iodides and Amines》, the research content is summarized as follows. A general copper-catalyzed carbonylative cross-coupling between amines and alkyl iodides was reported to form amides RC(O)NR1R2 [R = Cy, i-Pr, CH(Et)2, etc.; R1 = H, Me, R2 = n-hexyl, CH2Bn, t-Bu, etc.]. Using a simple combination of catalytic amounts of copper(I) chloride and N,N,N’;N”,N”-pentamethyldiethylenetriamine in the presence of sodium hydroxide under carbon monoxide pressure, a broad range of alkyl iodides and amines can be efficiently coupled to the corresponding amides that are obtained in good to excellent yields. Notable features of this process were the first one relying on a base metal catalyst, includeed the availability and low cost of the catalytic system, its successful use with primary, secondary, tertiary alkyl iodides and all classes of amines with no or limited competing nucleophilic substitution without CO incorporation as well as its efficiency with complex alkyl iodides and amines. Mechanistic studies demonstrated that a radical pathway is operative and the key role of CO.
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., SDS of cas: 104-86-9
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics