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  1. Feb 6, 2010 · Other names: N-Cyclohexylaniline; Benzenamine, N-cyclohexyl-; Aniline, N-cyclohexyl-; Cyclohexanamine, N-phenyl-; Cyclohexylamine, N-phenyl-; Diphenylamine, ar-hexahydro-; Cyclohexylphenylamine; N-Cyclohexylbenzenamine; Phenylcyclohexylamine; NSC 27510. Permanent link for this species.

  2. Oct 14, 2021 · Create: 2005-03-26. Modify: 2024-04-27. Description. 1-phenylcyclohexylamine is a DEA Schedule II controlled substance. Substances in the DEA Schedule II have a high potential for abuse which may lead to severe psychological or physical dependence. It is a Immediate precursors substance. Drug Enforcement Administration (DEA) 1 Structures.

  3. Other names: N-Cyclohexylaniline; Benzenamine, N-cyclohexyl-; Aniline, N-cyclohexyl-; Cyclohexanamine, N-phenyl-; Cyclohexylamine, N-phenyl-; Diphenylamine, ar-hexahydro-; Cyclohexylphenylamine; N-Cyclohexylbenzenamine; Phenylcyclohexylamine; NSC 27510

    • 1959/09/22
    • MONSANTO (J. FREEMAN)
    • N-cyclohexylanilineN-cyclohexyl-N-phenylamine
    • COBLENTZ NO. 08474
  4. 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.

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    • 6
  5. 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.

  6. Synthesis and anticonvulsant activity of 1-phenylcyclohexylamine analogs (PDF) Synthesis and anticonvulsant activity of 1-phenylcyclohexylamine analogs | Kenner Rice - Academia.edu Academia.edu no longer supports Internet Explorer.

  7. May 1, 1990 · Several analogues of 1-phenylcyclohexylamine (PCA), a phencyclidine (PCP) derivative, exhibited a greater separation of potencies in the motor toxicity and MES seizure tests than did the parent compound PCA. Expand. View on PubMed. doi.org. Save to Library. Create Alert. Cite. 41 Citations. Citation Type. More Filters.

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