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. Recommanded Product: (4-Chlorophenyl)methanamine.
Prajapati, Pankaj Kumar;Tripathi, Deependra;Poddar, Mukesh Kumar;Gupta, Piyush;Jain, Suman L. research published 《 Dual photocatalysis for CO2 reduction along with the oxidative coupling of benzylamines promoted by Cu/Cu2O@g-C3N4 under visible irradiation》, the research content is summarized as follows. The present work describes the twin functional photocatalysis promoted by a Cu/Cu2O decorated g-C3N4 heterojunction where the electrons at the Cu/Cu2O surface reduced CO2 to methanol selectively and holes facilitated oxidative coupling of benzylamines without any external sacrificial electron donors under ambient conditions. The heterojunction photocatalyst was prepared by refluxing g-C3N4 with copper precursors at 70°C. The structural and morphol. properties of the heterojunction were determined using XRD, FTIR, XPS, UV-vis, HR-TEM and PL spectroscopy. Photoelectrochem. measurements determined the electronic and photoactive properties. Following this twin strategy of CO2 utilization along with the oxidation of organic compounds into other valuable chems. in a single process may provide new opportunities for sustainable development and maintain the atom economy.
Recommanded Product: (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