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. Formula: C7H8ClN.
Yang, Hongchen;Zhang, Lu;Xu, Xiaoyong;Shao, Xusheng;Li, Zhong research published 《 Acid-Mediated Synthesis of Chromeno[2,3-b]pyridine Derivatives via Condensation of 2-Amino-3-formylchromones and 1-(Methylthio)-2-nitroenamine Derivatives》, the research content is summarized as follows. A convenient and effective protocol has been proposed for the synthesis of chromeno[2,3-b]pyridines I (R1 = H, i-Pr; R2 = Me, Et, PhCH2, etc.) via the CF3SO3H-catalyzed annulation of substituted 2-amino-3-formylchromones II and various 1-(methylthio)-2-nitroenamines R2NHC(SMe):CHNO2. This method is time-efficient, convenient, high-yielding and exhibits a good functional group compatibility.
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., Formula: C7H8ClN
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics