ChemicalBook--->CAS DataBase List--->195457-71-7

195457-71-7

195457-71-7 Structure

195457-71-7 Structure
IdentificationMore
[Name]

4'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID
[CAS]

195457-71-7
[Synonyms]

4-CARBOXY-4'-TRIFLUOROMETHYLDIPHENYL
4'-(TRIFLUOROMETHYL)[1,1'-BIPHENYL]-4-CARBOXYLIC ACID
4'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID
AKOS BAR-0023
RARECHEM AL BE 1218
4-(4-(Trifluoromethyl)phenyl)benzoic acid
4''-TRIFLUOROMETHYL-BIPHENYL-4-CARBOXYLIC ACID, 95+%
4'-Trifluoromethyl-biphenyl-4-carboxylic acid
[Molecular Formula]

C14H9F3O2
[MDL Number]

MFCD03424606
[Molecular Weight]

266.22
[MOL File]

195457-71-7.mol
Chemical PropertiesBack Directory
[Melting point ]

120.0-121.1 °C
[Boiling point ]

360.8±42.0 °C(Predicted)
[density ]

1.326±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

4.04±0.10(Predicted)
[color ]

White to Off-White
[CAS DataBase Reference]

195457-71-7(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[Hazard Note ]

Irritant
[HS Code ]

2916399090
Hazard InformationBack Directory
[Uses]

4''-(Trifluoromethyl)[1,1''-biphenyl]-4-carboxylic Acid is a reagent used in the synthesis of pharmaceuticals and pharmaceutical intermediates
[Synthesis]

4-Bromobenzoic acid

586-76-5

4-Trifluoromethylphenylboronic acid

128796-39-4

4'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID

195457-71-7

The general procedure for the synthesis of 4'-trifluoromethyl-diphenyl-4-carboxylic acid from 4-bromobenzoic acid and 4-trifluoromethylphenylboronic acid was as follows: the reaction was carried out according to General Method D. 4-Bromobenzoic acid (10 g, 49.4 mmol), 4-trifluoromethylphenylboronic acid (14.17 g, 74.61 mmol), tetrakis(triphenylphosphine)palladium (5.7 g, 4.974 mmol) and 2N Na2CO3 aqueous solution (150 mL, 149.2 mmol) were mixed in 500 mL of toluene. Upon completion of the reaction, the reaction mixture was neutralized with 2N HCl and subsequently filtered. The resulting solid was dissolved in ethyl acetate and purified by a short silica gel column to give 9.7 g (75% yield) of the target product 4'-trifluoromethyl-diphenyl-4-carboxylic acid as a white solid.

[References]

[1] Tetrahedron Letters, 2005, vol. 46, # 34, p. 5751 - 5754
[2] Green Chemistry, 2010, vol. 12, # 1, p. 150 - 158
[3] Patent: WO2004/14844, 2004, A2. Location in patent: Page 179; 181
[4] Journal of Medicinal Chemistry, 2007, vol. 50, # 20, p. 4939 - 4952
[5] Journal of Medicinal Chemistry, 1997, vol. 40, # 20, p. 3144 - 3150
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