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Feb 6, 2010 · Data from NIST Standard Reference Database 69: NIST Chemistry WebBook The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment.
Oct 14, 2021 · NIH. HHS. 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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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 ).
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- 1959/09/22
- MONSANTO (J. FREEMAN)
- N-cyclohexylanilineN-cyclohexyl-N-phenylamine
- COBLENTZ NO. 08474
Feb 6, 2010 · 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 IUPAC Standard InChIKey: TXTHKGMZDDTZFD-UHFFFAOYSA-N ...
Jul 31, 2007 · Cyclohexanes. Cycloparaffins. Chemical Taxonomy Provided by Classyfire. Description. This compound belongs to the class of organic compounds known as aralkylamines. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group. Kingdom.
Aug 27, 2020 · Exercise 24.4.1. Using the knowledge of the electron donating or withdrawing effects of subsituents gained in Section 16.6, rank the following compound in order of decreasing basicity. a) p -Nitroaniline, methyl p-aminobenzoate, p -chloroaniline. b) p -Bromoaniline, p -Aminobenzonitrile, p -ethylaniline.
