3-(Trifluoromethyl)aniline, 99%

Name: 3-(Trifluoromethyl)aniline, 99%
SKU: A15910.36

CAS: 98-16-8 | C7H6F3N | 161.127 g/mol

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產品號碼 A15910.36

亦稱為 A15910-36

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500 g

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化學識別

CAS98-16-8

IUPAC Name3-(trifluoromethyl)aniline

Molecular FormulaC7H6F3N

InChI KeyVIUDTWATMPPKEL-UHFFFAOYSA-N

SMILESNC1=CC=CC(=C1)C(F)(F)F

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規格

規格表

Appearance (Color)Clear colorless to yellow to orange

Assay (GC)≥98.5%

Refractive Index1.4785-1.4815 @ 20°C

FormLiquid

Identification (FTIR)Conforms

Used as pharmaceutical intermediate.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Used as pharmaceutical intermediate.

Solubility
Soluble in water. [5 g/L (20°C)]

Notes
Store in cool dry place. Keep away from oxidizing agents.

RUO – Research Use Only

General References:

Domenico Spinelli .; Paolo Zanirato.; Elvira Di Miceli.; Liliana Lamartina.;Francesco Guerrera. On the Reaction of 3-Bromo-2-nitrobenzo[b]thiophene 13C-Labeled at C-2 with 3-(Trifluoromethyl)aniline: A Preliminary Insight into a Nucleophilic Substitution with Rearrangement. J. Org. Chem. 1997, 62 (15), 4921-4923 .
V. Arjunan.; T. Rani.; S. Mohan. Spectroscopic and quantum chemical electronic structure investigations of 2-(trifluoromethyl)aniline and 3-(trifluoromethyl)aniline.J. Mol. Struct. 2011, (1-3), 179-193 .
Used in an example of a general method for the conversion of aromatic amines to sulfonyl chlorides by reaction of the diazonium chlorides with SO₂: Org. Synth. Coll., 7, 508 (1990).