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Benzylamine, also known as phenylmethylamine, is an organic chemical compound with the condensed structural formula C 6 H 5 CH 2 NH 2 (sometimes abbreviated as PhCH 2 NH 2 or BnNH 2). It consists of a benzyl group, C 6 H 5 CH 2, attached to an amine functional group , NH 2 .
N,N-Dimethylbenzylamine can be synthesized by the Eschweiler–Clarke reaction of benzylamine [2] [3] ... Safety MSDS data Archived 2007-10-11 at the Wayback Machine
N-isopropylbenzylamine is a compound that has appeared in chemical literature often playing an intermediary role in applications of experimental synthesis and novel organic transformations.
Industrially, benzyl chloride is the precursor to benzyl esters, which are used as plasticizers, flavorants, and perfumes. Phenylacetic acid, a precursor to pharmaceuticals, is produced from benzyl cyanide, which in turn is generated by treatment of benzyl chloride with sodium cyanide.
Pargyline is an derivative of benzylamine and is also known as N-methyl-N-propargylbenzylamine. [13] [48] It is used pharmaceutically as the hydrochloride salt. [4] [5] [13] Pargyline is a lipophilic compound, with a predicted log P of about 2.1. [48] [26]
Benzalkonium chloride (BZK, BKC, BAK, BAC), also known as alkyldimethylbenzylammonium chloride (ADBAC) and by the trade name Zephiran, [1] is a type of cationic surfactant.It is an organic salt classified as a quaternary ammonium compound.
Benzamidine is a reversible competitive inhibitor of trypsin, trypsin-like enzymes, and serine proteases. [4]It is often used as a ligand in protein crystallography to prevent proteases from degrading a protein of interest.
Benzal chloride is produced by the free radical chlorination of toluene, being preceded in the process by benzyl chloride (C 6 H 5 CH 2 Cl) and followed by benzotrichloride (C 6 H 5 CCl 3):