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196886

Sigma-Aldrich

2-(Trifluoromethyl)benzoic acid

98%

Sinónimos:

α,α,α-Trifluoro-o-toluic acid, 2-Carboxybenzotrifluoride

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About This Item

Fórmula lineal:
CF3C6H4CO2H
Número de CAS:
433-97-6
Peso molecular:
190.12
Beilstein/REAXYS Number:
976984
EC Number:
207-093-9
MDL number:
MFCD00002476
UNSPSC Code:
12352100
PubChem Substance ID:
24851804
NACRES:
NA.22

assay

98%

form

solid

bp

247 °C/753 mmHg (lit.)

mp

107-110 °C (lit.)

functional group

carboxylic acid
fluoro

SMILES string

OC(=O)c1ccccc1C(F)(F)F

InChI

1S/C8H5F3O2/c9-8(10,11)6-4-2-1-3-5(6)7(12)13/h1-4H,(H,12,13)

InChI key

FBRJYBGLCHWYOE-UHFFFAOYSA-N

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Categorías relacionadas

Application

2-(Trifluoromethyl)benzoic acid was used in the synthesis of 1,3,4-oxadiazole derivatives containing 2-fluoro-4-methoxy moiety. It was also used to investigate the binding of 2-pyridinone and amino acid derivative as ligands with chaperones PapD and FimC by surface plasmon resonance and 1HNMR spectroscopy.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
MKCG4107
MKCC0447
MKBV8578V
MKBQ8335V
MKBP3429V

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B Chandrakantha et al.
European journal of medicinal chemistry, 45(3), 1206-1210 (2009-12-17)
In the present study a series of new 1,3,4-oxadiazole derivatives containing 2-fluoro-4-methoxy moiety were synthesized. These newly synthesized compounds were characterized by NMR, mass spectral, IR spectral study and also by C, H, N analyses. All the newly synthesized compounds
Tobias Tengel et al.
Organic & biomolecular chemistry, 2(5), 725-731 (2004-02-27)
Identification of compounds from chemical libraries that bind to macromolecules by use of NMR spectroscopy has gained increasing importance during recent years. A simple methodology based on (19)F NMR spectroscopy for the screening of ligands that bind to proteins, which
R D Farrant et al.
Journal of pharmaceutical and biomedical analysis, 13(8), 971-977 (1995-07-01)
Many drugs containing carboxylic acid functional groups are metabolised in vivo to ester glucuronides (1-O-acyl-beta-D-glucopyranuronates) and, of these, a number show a propensity to undergo internal isomerisation via a transacylation process, causing the carboxylic acid moiety to migrate successively to
Studies on the metabolism of fluorinated xenobiotics in the rat using 19F-NMR and 1H-NMR spectroscopy.
F Y Ghauri et al.
Journal of pharmaceutical and biomedical analysis, 8(8-12), 939-944 (1990-01-01)

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