3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID
3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID Basic information
- Product Name:
- 3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID
- Synonyms:
-
- 3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID
- 3'-(TRIFLUOROMETHYL)-1,1'-BIPHENYL-4-CARBOXYLIC ACID
- AKOS BAR-0024
- [1,1'-BIPHENYL]-4-CARBOXYLIC ACID, 3'-(TRIFLUOROMETHYL)-
- RARECHEM AL BE 1367
- 4-(3-(Trifluoromethyl)phenyl)benzoic acid
- 4-[3-(trifluoromethyl)phenyl]benzoate
- 3'-(Trifluoromethyl)[1,1'-biphenyl]-4-carboxylic acid
- CAS:
- 195457-70-6
- MF:
- C14H9F3O2
- MW:
- 266.22
- Product Categories:
-
- pharmacetical
- Mol File:
- 195457-70-6.mol
3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID Chemical Properties
- storage temp.
- Sealed in dry,Room Temperature
- form
- solid
- color
- Yellow
- CAS DataBase Reference
- 195457-70-6(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Hazard Note
- Irritant
- HS Code
- 2916399090
3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID Usage And Synthesis
Uses
4-(3-Trifluoromethylphenyl)benzoic Acid is a reagent used in the synthesis of aryl-substituted aspartic acid and diaminopropionic acid derivatives as inhibitors of glutamate transporter EAAT-2 (Excitatory amino acid transporters 2).
Synthesis
586-76-5
1423-26-3
195457-70-6
The general procedure for the synthesis of 4-(3-trifluoromethylphenyl)benzoic acid from 4-bromobenzoic acid and 3-(trifluoromethyl)phenylboronic acid was as follows: Pd(dppf)Cl2 (1.49 mmol, 1.09 g) was added to a mixture containing 4-bromobenzoic acid (14.9 mmol, 3.0 g), 3-(trifluoromethyl)phenylboronic acid (17.9 mmol, 3.4 g), and Cs2CO3 (37.3 mmol, 12.2 g) in a suspension with the solvent being a mixture of 30 mL dioxane and 7.5 mL ethanol. The reaction mixture was stirred at 80 °C for 2 hours. After completion of the reaction, it was cooled to room temperature, the solid product was collected by filtration and washed with methanol. The filtrate was concentrated and the residue was partitioned between ethyl acetate and 1N aqueous hydrochloric acid. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. To the concentrated residue was added dichloromethane, the resulting solid was collected by filtration, washed with dichloromethane and dried to give 4-(3-trifluoromethylphenyl)benzoic acid (3.58 g, 86% yield), which could be used in the next reaction without further purification.
References
[1] Patent: US2013/102584, 2013, A1. Location in patent: Paragraph 0307; 0308
[2] Journal of Medicinal Chemistry, 1997, vol. 40, # 20, p. 3144 - 3150
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3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID(195457-70-6)Related Product Information
- 3-(TRIFLUOROMETHYL)BIPHENYL
- 3'-TRIFLUOROMETHYLBIPHENYL-3-CARBOXYLIC ACID
- 2'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID,Trifluoromethylbiphenyl-4-carboxylic acid
- 4'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID
- 4'-FLUORO-3'-TRIFLUOROMETHYL-BIPHENYL-4-CARBOXYLIC ACID
- 3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID
- RARECHEM AL BI 1367
- AKOS BAR-2150
- 3',5'-DI-(TRIFLUOROMETHYL)-BIPHENYL-4-CARBOXYLIC ACID
- 3-fluoro-3'-(trifluoromethyl)-1,1'-biphenyl-4-carboxylic acid
- METHYL 3'-(TRIFLUOROMETHYL)[1,1'-BIPHENYL]-4-CARBOXYLATE
- AKOS BAR-2112
- AKOS BAR-2103
- METHYL 4'-NITRO-3'-(TRIFLUOROMETHYL)[1,1'-BIPHENYL]-4-CARBOXYLATE