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  1. Jan 1, 2016 · The first arylcyclohexamine to be described was 1-(1-phenylcyclohexyl) amine, in 1907, almost 50 years before the synthesis of PCP . Other analogues reported in the early 1950s included N -ethyl-1-phenylcyclohexylamine (PCE) and 1-(1-phenylcyclohexyl)morpholine (PCMo).

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      Arylcyclohexamines (also known as arylcyclohexylamines) are...

  2. The Synthesis of Phencyclidine and Other 1--4rylcyclohexylamines Received Juniiary 10, 1964 Revised Manuscripi Received October 2 $, 1!64 \-arious 1-arylcyclohesylaniiiies were synthesized fur evaliiatioii :ti ceiitral nervous system depressants. The compounds were prepared by several procedures.

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  4. Phencyclidine (PCP) is believed to be the first arylcyclohexylamine with recognized anesthetic properties, but several arylcyclohexylamines were described before PCP in the scientific literature, beginning with PCA (1-phenylcyclohexan-1-amine) the synthesis of which was first published in 1907.

    Compound
    Aryl Substituent
    N Group
    Cyclohexyl Ring
    2-HO-PCP
    Phenyl
    Piperidine
    2-Hydroxy
    2-Me-PCP
    Phenyl
    Piperidine
    2-Methyl
    2-MeO-PCP
    Phenyl
    Piperidine
    2-Methoxy
    2-Keto-PCP
    Phenyl
    Piperidine
    2-Keto
  5. Apr 2, 2013 · Preparation and analytical characterization of 1‐ (1phenylcyclohexyl)piperidine (PCP) and 1‐ (1phenylcyclohexyl)pyrrolidine (PCPy) analogues - Wallach - 2014 - Drug Testing and Analysis - Wiley Online Library.

    • Jason Wallach, Giorgia De Paoli, Adeboye Adejare, Simon D. Brandt
    • 2014
  6. 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.

  7. May 1, 1990 · Thirty-eight analogues of 1-phenylcyclohexylamine (PCA), a phencyclidine (PCP) derivative, were examined for their activities in the mouse maximal electroshock (MES) seizure test and in a motor-toxicity assay.

  8. 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. IUPAC Standard InChIKey: TXTHKGMZDDTZFD-UHFFFAOYSA-N. CAS Registry Number: 1821-36-9. Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file.

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