CAS 25753-22-4

2,4,6-tris(trifluoromethyl)aniline

Description:

2,4,6-Tris(trifluoromethyl)aniline is an aromatic amine characterized by the presence of three trifluoromethyl groups attached to the aniline structure at the 2, 4, and 6 positions of the benzene ring. This compound is notable for its high electronegativity due to the trifluoromethyl groups, which can significantly influence its chemical reactivity and physical properties. It typically appears as a solid at room temperature and is soluble in organic solvents. The presence of the trifluoromethyl groups enhances its lipophilicity and can affect its interactions with biological systems, making it of interest in various fields, including materials science and pharmaceuticals. Additionally, the compound may exhibit unique thermal and chemical stability due to the strong C-F bonds. Safety considerations are important, as many trifluoromethylated compounds can be toxic or environmentally persistent. Proper handling and disposal methods should be employed when working with this substance.

Formula: C₉H₄F₉N

InChI: InChI=1/C9H4F9N/c10-7(11,12)3-1-4(8(13,14)15)6(19)5(2-3)9(16,17)18/h1-2H,19H2

SMILES: c1c(cc(c(c1C(F)(F)F)N)C(F)(F)F)C(F)(F)F

2,4,6-Tris(trifluoromethyl)aniline

CAS: 25753-22-4

2,4,6-Tris(trifluoromethyl)aniline

Purity: ≥95%

Molecular weight: 297.12g/mol

Ref: 54-PC8560

2,4,6-Tris(trifluoromethyl)aniline

CAS: 25753-22-4

Formula: C₉H₄F₉N

Purity: 97.0%

Molecular weight: 297.124

Ref: 10-F064735

2,4,6-Tris(trifluoromethyl)aniline

Controlled Product

CAS: 25753-22-4

Applications 2,4,6-Tris(trifluoromethyl)aniline, is a Fluorinated substituents that have become valuable tool in medical chemistry. It can also be used for the preparation of azo dyes containing fluorine.
References Gandel'sman, L. Z., et al.: Ukrainskii Khimicheskii , 41, 61 (1975); Edelbach, B. L., et al.: Synthesis, 44, 3595 (2012);

Formula: C₉H₄F₉N

Color and Shape: Neat

Molecular weight: 297.12

Ref: TR-T876695