3-Amino-5-(trifluoromethyl)benzoic acid
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
- 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 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
- pka
- 3.93±0.10(Predicted)
- color
- Light yellow to Yellow to Orange
- CAS DataBase Reference
- 328-68-7(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
3-Amino-5-(trifluoromethyl)benzoic acid Usage And Synthesis
Uses
peptide synthesis
reaction suitability
reaction type: solution phase peptide synthesis
Synthesis
328-80-3
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
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