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  1. 2022-01-15. Create. 2005-03-26. 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. Drug Enforcement Administration (DEA)

    • C12H17N
    • 31.9K
    • 175.27
  2. phenylcyclohexylamine water salt Prior art date 1960-04-04 Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

  3. phenylcyclohexylamine water salt Prior art date 1960-04-04 Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.) Expired - Lifetime Application number US19477A Inventor Erik F Godefroi Robert F Parcell

    • Erik F Godefroi, Robert F Parcell
    • 2
    • 1960
  4. The manufacture of PCP is a simple process; it requires little formal chemica.l training and laboratory apparatus. As true in any chemical synthesis, the precursor chemicals themselves produce PCP when combined correctly. PCP is produced in both liquid and powder forms.

  5. Find Similar Structures. Chemical Safety. Laboratory Chemical Safety Summary (LCSS) Datasheet. Molecular Formula. C12H17N. Synonyms. 4-phenylcyclohexanamine. 19992-45-1. 4-Phenylcyclohexylamine.

    • C12H17N
    • 29.9K
  6. phenylcyclohexylamine water salt Prior art date 1960-04-04 Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

  7. Synthesis and anticonvulsant activity of 1-phenylcyclohexylamine analogues. 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. In addition, we determined the binding affinities of the compounds for PCP acceptor sites ….

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