Yahoo Web Search

Search results

  1. 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.

  2. For Zoom; 1.) Enter the desired X axis range (e.g., 100, 200) 2.) Check here for automatic Y scaling 3.) Press here to zoom

    • 1959/09/22
    • MONSANTO (J. FREEMAN)
    • N-cyclohexylanilineN-cyclohexyl-N-phenylamine
    • COBLENTZ NO. 08474
  3. People also ask

  4. 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). While many were not explored further by their initial investigators, chemists ...

  5. An arylcyclohexylamine is composed of a cyclohexylamine unit with an aryl moiety attachment. The aryl group is positioned geminal to the amine. In the simplest cases, the aryl moiety is typically a phenyl ring, sometimes with additional substitution. The amine is usually not primary; secondary amines such as methylamine or ethylamine, or ...

  6. May 13, 2021 · Here are just a few examples. Double addition of phenyl Grignard to an ester. A Clemmensen reduction (which doesn’t touch the carboxylic acid) ( Org Syn. Coll. Vol. 2, p. 499) A classic Claisen condensation ( Org. Syn. Coll. Vol 3. p. 17 ) It’s one thing to make reactions up for a test (and of course necessary from time to time) ; it’s ...

  7. Apr 2, 2013 · Drug Testing and Analysis is a specialist journal covering sports doping, recreational drugs, pharmaceuticals, toxico-pathology, forensics, and the environment.

  8. 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.

  1. People also search for