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Feb 6, 2010 · N-Phenylcyclohexylamine. Formula: C 12 H 17 N. Molecular weight: 175.2701. IUPAC Standard InChI: InChI=1S/C12H17N/c1-3-7-11 (8-4-1)13-12-9-5-2-6-10-12/h1,3-4,7-8,12-13H,2,5-6,9-10H2. Copy Sheet of paper on top of another sheet. IUPAC Standard InChIKey: TXTHKGMZDDTZFD-UHFFFAOYSA-N.
Oct 14, 2021 · USA.gov. 1-Phenylcyclohexylamine | C12H17N | CID 31862 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
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What are arylcyclohexamines?
Jan 1, 2016 · The most well-characterized arylcyclohexamines are phencyclidine ( (1- (1-phencyclohexyl) piperidine; PCP )), ketamine, and, of the novel analogues, methoxetamine. Fig. 1. Chemical structures of the primary arylcyclohexamines: phencyclidine , ketamine , and methoxetamine. Full size image.
thesis of 1-phenylcyclohexylamine. The compound prepared by the alternate route (method F) was identi- cal in all respects with the one obtained prepared from Method F aC6"I NCO - CxCeH5 "2 VI phenylcyclohexene. Recently, Cristol, et ul., re- ported the isolation of the amine as its benzoyl deriva- tive via a modified Ritter reaction.
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A series of phencyclidine homologs was synthesized by reductive cyclization of substituted ω-chlorine-substituted l-N- [l- (p-hydroxybenzyl)cyclohexyl]amides with LiAlH4 by characterized and tested for neurotropic activity. Expand. 1. Synthesis and biological activity of cyclohexylamine derivatives. V. A. Glushkov O. S. P’yankova. +4 authors.
Cyclohexylamine is used as an intermediate in synthesis of other organic compounds. It is the precursor to sulfenamide -based reagents used as accelerators for vulcanization. It is a building block for pharmaceuticals (e.g., mucolytics, analgesics, and bronchodilators ). The amine itself is an effective corrosion inhibitor.
Synthesis of deuterium‐labelled drugs of abuse for use as internal standards in quantification by selected ion monitoring. I. Methamphetamine; 2,5‐dimethoxy‐4‐methylamphetamine (DOM); phencyclidine (PCP); and methaqualone. Journal of Labelled Compounds and Radiopharmaceuticals 1976, 12 (1) , 69-78.
