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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] ... This page was last edited on 1 February 2024, at 22:19 (UTC).
Isopropylbenzylamine hydrochloride crystals seized by DEA. References This page was last edited on ... This page was last edited on 13 August 2024, at 01:04 (UTC).
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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.
1-Phenylethylamine may be prepared by the reductive amination of acetophenone: [1]. C 6 H 5 C(O)CH 3 + NH 3 + H 2 → C 6 H 5 CH(NH 2)CH 3 + H 2 O. The Leuckart reaction, using ammonium formate, is another method for this transformation.
In an 84-page statement of claim filed in Ontario's superior court of justice, the five Canadian companies demanded damages from OpenAI and a permanent injunction preventing it from using their ...
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]
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