The class of organic compounds having covalently a bonded chlorine atom is called organic chlorides. 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 named reactions and applications. Recommanded Product: (4-Chlorophenyl)methanamine.
Zengin Karadayi, Fikriye;Basaran, Rahman;Kisla, Mehmet Murat;Can Eke, Binay;Ates Alagoz, Zeynep research published 《 Synthesis, antioxidant activity, molecular docking and ADME studies of novel pyrrolebenzimidazole derivatives》, the research content is summarized as follows. Several 5-(alkylsulfonyl)-1-substituted-2-(1H-pyrrol-2-yl)-1H-benzo[d]imidazole derivatives I [R1 = Me, Et, n-Pr; R2 = Me, n-Bu, Bn, etc.] were synthesized and their antioxidant activities were investigated using lipid peroxidation (LPO) and 7-ethoxyresorufin O-deethylase (EROD) assays. Docking anal. with human NAD[P]H-Quinone oxidoreductase 1 (NQO1) was also performed to gather thorough information about these compounds I that have antioxidant activities. Moreover, their mol. descriptors and ADME properties were calculated using the SwissADME online program. As a result, most of compounds I possessed better affinity and created ample interactions with NQO1. The most potent compound I [R1 = Et; R2 = Bn] had LP inhibition value of 3.73 nmol/mg/min. Other compounds I exhibited moderate activity on LP levels comparing to standard butylated hydroxy toluene (BHT). However, the inhibitory effect on EROD activity was not significant.
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., Recommanded Product: (4-Chlorophenyl)methanamine
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics