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3-Amino-5-(trifluoromethyl)benzoic acid

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3-Amino-5-(trifluoromethyl)benzoic acid manufacturers

3-Amino-5-(trifluoromethyl)benzoic acid Basic information
Product Name:3-Amino-5-(trifluoromethyl)benzoic acid
Synonyms:3-Amino-5-carboxybenzotrifluoride, 3-Carboxy-5-(trifluoromethyl)aniline;3-Amino-5-(trifluoromethyl)benzoic acid 97%;3-AMINO-5-(TRIFLUOROEMTHYL)BENZOIC ACID;3-Amino-5-(trifluoromethyl)benzoicacid97%;BUTTPARK 25\01-23;3-AMINO-5-(TRIFLUOROMETHYL)BENZOIC ACID;3-Amino-5-(trifluoromethyl)benzoic Acid >;Benzoic acid, 3-amino-5-(trifluoromethyl)-
CAS:328-68-7
MF:C8H6F3NO2
MW:205.13
EINECS:
Product Categories:Fluorine series;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Benzoic acid;Aromatic Amino Acids;Peptide Synthesis;Unnatural Amino Acid Derivatives
Mol File:328-68-7.mol
3-Amino-5-(trifluoromethyl)benzoic acid Structure
3-Amino-5-(trifluoromethyl)benzoic acid Chemical Properties
Melting point 141-146 °C(lit.)
Boiling point 331.9±42.0 °C(Predicted)
density 1.489±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form powder to crystal
pka3.93±0.10(Predicted)
color Light yellow to Yellow to Orange
Major Applicationpeptide synthesis
InChI1S/C8H6F3NO2/c9-8(10,11)5-1-4(7(13)14)2-6(12)3-5/h1-3H,12H2,(H,13,14)
InChIKeyWBTHOSZMTIPJLR-UHFFFAOYSA-N
SMILESNc1cc(cc(c1)C(F)(F)F)C(O)=O
CAS DataBase Reference328-68-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
RTECS DD6205700
HazardClass IRRITANT
HS Code 2934999090
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
3-Amino-5-(trifluoromethyl)benzoic acid Usage And Synthesis
Usespeptide synthesis
reaction suitabilityreaction type: solution phase peptide synthesis
Synthesis
3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID

328-80-3

3-Amino-5-(trifluoromethyl)benzoic acid

328-68-7

The suspension formed by 3-nitro-5-(trifluoromethyl)benzoic acid (103 g x 2 batches) obtained in step 1 and 10% palladium-carbon catalyst (5.15 g x 2 batches) in ethanol (1500 mL x 2 batches) was placed under the atmosphere of hydrogen at 1 atmospheric pressure, and the reaction was stirred for 7 hours at room temperature. After completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to afford the target product 3-amino-5-(trifluoromethyl)benzoic acid (180 g, 100% yield) as a light yellow powder. The product was characterized by 1H-NMR (300 MHz, CDCl3): δ 4.00-6.00 (2H, broad peak), 7.10 (1H, single peak), 7.53 (1H, single peak), 7.72 (1H, single peak).

References[1] Patent: US2008/275085, 2008, A1. Location in patent: Page/Page column 45
[2] Chemistry - A European Journal, 2017, vol. 23, # 52, p. 12758 - 12762
[3] Patent: US2007/213371, 2007, A1. Location in patent: Page/Page column 70
[4] Journal of the American Chemical Society, 2017, vol. 139, # 43, p. 15308 - 15311
[5] Patent: WO2004/29038, 2004, A1. Location in patent: Page 44
3-Amino-5-(trifluoromethyl)benzoic acid Preparation Products And Raw materials
Raw materials3-Nitro-5-(trifluoromethyl)benzoic acid-->Hydrogen-->Ethanol
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