CAS 455-14-1
:4-(Trifluorometil)anilina
- 4-Aminobenzotrifluoride
- p-Trifluoromethylaniline
- Trifluoromehylphenylanilide
- 4-Trifluoromethyl Aniline
- 4-Amino Trifluorotoluene
- Aminobenzotrifluoride, 4-
- (4-(Trifluoromethyl)phenyl)amine
- 1-Amino-4-(trifluoromethyl)benzene
- 4-(Trifluoromethyl)benzenamine
- 4-Amino-α,α,α-benzotrifluoride
- Benzenamine, 4-(trifluoromethyl)-
- Benzotrifluoride, 4-Amino-
- Nsc 10337
- p-(Trifluoromethyl)aniline
- p-Aminobenzotrifluoride
- p-Amino-α,α,α-trifluorotoluene
- p-Toluidine, α,α,α-trifluoro-
- p-Trifluoromethylphenylamine
- α,α,α-Trifluoro-p-toluidine
- α,α,α-Trifluor-p-toluidin
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4-Aminobenzotrifluoride
CAS:Fórmula:C7H6F3NPureza:>98.0%(GC)(T)Forma y color:Colorless to Light orange to Yellow clear liquidPeso molecular:161.134-Aminobenzotrifluoride
CAS:4-AminobenzotrifluorideFórmula:C7H6F3NPureza:97%Forma y color:Yellow LiquidPeso molecular:161.124444-(Trifluoromethyl)aniline-2,3,5,6-d4
CAS:Fórmula:CF3C6D4NH2Pureza:98 atom % DForma y color:Colorless To Brown LiquidPeso molecular:165.070344-(Trifluoromethyl)aniline
CAS:Producto controladoImpurity Leflunomide EP Impurity A; Leflunomide USP Related Compound A
Applications 4-(Trifluoromethyl)aniline (Leflunomide EP Impurity A; Leflunomide USP Related Compound A) is a 4-Substituted aniline derivatives exert 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),Fórmula:C7H6F3NForma y color:NeatPeso molecular:161.124-(Trifluoromethyl)aniline
CAS:4-(Trifluoromethyl)anilineFórmula:C7H6F3NPureza:98%Peso molecular:161.124-Aminobenzotrifluoride
CAS:4-Aminobenzotrifluoride is a chemical compound that belongs to the group of nitroso compounds. It has been shown to have antiproliferation activity in vitro and in vivo. 4-Aminobenzotrifluoride is synthesized by reacting sodium nitrite with p-hydroxybenzoic acid in the presence of an organic acid, such as acetic acid or formic acid, to produce diazonium salt. The diazonium salt is then reacted with an inorganic acid, such as hydrochloric acid or sulfuric acid. This reaction produces 4-aminobenzotrifluoride and water.
Fórmula:C7H6F3NPureza:Min. 95%Forma y color:Clear LiquidPeso molecular:161.12 g/molLeflunomide Related Compound A
CAS:Toluidines (aminotoluenes) and their derivatives, salts thereofFórmula:C7H6F3NForma y color:Colorless Light Yellow LiquidPeso molecular:161.04523












