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3-(Trifluoromethyl)aniline, 99%, Thermo Scientific Chemicals
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Catalog number A15910.36
also known as A15910-36
Price (USD)/ Each
85.65
Online exclusive
95.10 Save 9.45 (10%)
-
Quantity:
500 g
Price (USD)/ Each
85.65
Online exclusive
95.10 Save 9.45 (10%)
3-(Trifluoromethyl)aniline, 99%, Thermo Scientific Chemicals
Catalog numberA15910.36
Price (USD)/ Each
85.65
Online exclusive
95.10 Save 9.45 (10%)
-
Chemical Identifiers
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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Specifications
Specification Sheet
Specification SheetAppearance (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.
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).