CymitQuimica logo

CAS: 1219795-48-8

Sort by

Found 5 products.
  • 4-(Trifluoromethyl)aniline-2,3,5,6-d4

    Controlled Product
    CAS:
    Formula:C72H4H2F3N

    Ref: TR-CDN-D-5606-0.1G

    100mg
    603.00€
  • 4-(Trifluoromethyl)aniline-2,3,5,6-d4

    CAS:
    Formula:CF3C6D4NH2
    Purity:98 atom % D
    Color and Shape:Colorless To Brown Liquid
    Molecular weight:165.07034

    Ref: 3U-D5606

    100mg
    658.00€
    250mg
    1,260.00€
  • 4-(Trifluoromethyl)aniline-d4

    Controlled Product
    CAS:
    Applications Isotope labelled 4-(Trifluoromethyl)aniline, a substituted aniline derivative that exerts special hematotoxicity on the red blood cells and induce leukocytosis. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Weber, W., et al.: Pharmacol. Rev., 37, 25 (1985), Hein, D., et al.: Carcinogenesis, 14, 1633 (1993), Payton, M., et al.: Microbiology, 147, 1137 (2001), Mushtaq, A., et al.: J. Biol. Chem., 277, 12175 (2002),
    Formula:C7H2D4F3N
    Color and Shape:Neat
    Molecular weight:165.15

    Ref: TR-T791052

    10mg
    245.00€
  • 4-(Trifluoromethyl)aniline-2,3,5,6-d4

    Controlled Product
    CAS:
    Formula:C72H4H2F3N

    Ref: TR-CDN-D-5606

    250mg
    1,121.00€
  • 4-(Trifluoromethyl)aniline

    CAS:
    4-(Trifluoromethyl)aniline is a non-aromatic amine that can be prepared by the elimination of propiophenone. It can also be synthesized with a Grignard reagent and iminium ion. 4-(Trifluoromethyl)aniline undergoes an electrophilic substitution reaction with triflic acid to form an iminium ion, which then reacts with a nucleophile to form an imine. The mechanism for this reaction is unclear and has been studied extensively using magnetic resonance spectroscopy (NMR), x-ray diffraction data, and other techniques.
    Formula:C7H2D4F3N
    Purity:Min. 95%
    Molecular weight:165.15 g/mol

    Ref: 3D-FT78397

    ne
    Discontinued
    Discontinued product