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454-92-2

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454-92-2 Usage

Chemical Properties

White to light yellow crystal powde

Definition

ChEBI: A benzoic acid carrying a trifluoromethyl substituent at the 3-position.

General Description

pKa values of 3-(trifluoromethyl)benzoic acid in water and in methanol has been measured. Solubility of 3-(trifluoromethyl)benzoic acid in dense carbon dioxide was evaluated to investigate the influence of fluorination on the solubility of organic pharmaceuticals in dense carbon dioxide.

Check Digit Verification of cas no

The CAS Registry Mumber 454-92-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 454-92:
(5*4)+(4*5)+(3*4)+(2*9)+(1*2)=72
72 % 10 = 2
So 454-92-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H5F3O2/c9-8(10,11)6-3-1-2-5(4-6)7(12)13/h1-4H,(H,12,13)/p-1

454-92-2 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (A16737)  3-(Trifluoromethyl)benzoic acid, 98+%   

  • 454-92-2

  • 10g

  • 464.0CNY

  • Detail
  • Alfa Aesar

  • (A16737)  3-(Trifluoromethyl)benzoic acid, 98+%   

  • 454-92-2

  • 50g

  • 1667.0CNY

  • Detail
  • Alfa Aesar

  • (A16737)  3-(Trifluoromethyl)benzoic acid, 98+%   

  • 454-92-2

  • 250g

  • 6388.0CNY

  • Detail

454-92-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-trifluoromethylbenzoic acid

1.2 Other means of identification

Product number -
Other names 3-trifluoromethylbenzoicacid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:454-92-2 SDS

454-92-2Relevant articles and documents

Aerobic oxidation of aldehydes to carboxylic acids catalyzed by recyclable ag/c3 n4 catalyst

Wu, Chaolong,Yao, Xiaoquan,Yu, Min,Zhou, Li,Zhu, Li

, p. 167 - 175 (2021/03/19)

The oxidation of aldehydes is an efficient methodology for the synthesis of carboxylic acids. Herein we hope to report a simple, efficient and recyclable protocol for aerobic oxidation of aldehydes to carboxylic acid by using C3N4 supported silver nanoparticles (Ag/C3N4) as a catalyst in aqueous solution under mild conditions. Under standard conditions, the corresponding carboxylic acids can be obtained in good to excellent yields. In addition, Ag/C3N4 is convenient for recovery and could be reused three times with satisfactory yields.

Hydrolysis of amides to carboxylic acids catalyzed by Nb2O5

Siddiki,Rashed, Md. Nurnobi,Touchy, Abeda Sultana,Jamil, Md. A. R.,Jing, Yuan,Toyao, Takashi,Maeno, Zen,Shimizu, Ken-Ichi

, p. 1949 - 1960 (2021/03/26)

Hydrolysis of amides to carboxylic acids is an industrially important reaction but is challenging due to the difficulty of cleaving the resonance stabilized amidic C-N bond. Twenty-three heterogeneous and homogenous catalysts were examined in the hydrolysis of acetamide. Results showed that Nb2O5was the most effective heterogeneous catalyst with the greatest yield of acetic acid. A series of Nb2O5catalysts calcined at various temperatures were characterized and tested in the hydrolysis of acetamide to determine the effects of crystal phase and surface properties of Nb2O5on catalytic performance. The high catalytic performance observed was attributed mainly to the facile activation of the carbonyl bond by Lewis acid sites that function even in the presence of basic inhibitors (NH3and H2O). The catalytic studies showed the synthetic advantages of the present method, such as simple operation, catalyst recyclability, additive free, solvent free, and wide substrate scope (>40 examples; up to 95% isolated yield).

Cobalt-catalyzed carboxylation of aryl and vinyl chlorides with CO2

Wang, Yanwei,Jiang, Xiaomei,Wang, Baiquan

supporting information, p. 14416 - 14419 (2020/12/01)

The transition-metal-catalyzed carboxylation of aryl and vinyl chlorides with CO2 is rarely studied, and has been achieved only with a Ni catalyst or combination of palladium and photoredox. In this work, the cobalt-catalyzed carboxylation of aryl and vinyl chlorides and bromides with CO2 has been developed. These transformations proceed under mild conditions and exhibit a broad substrate scope, affording the corresponding carboxylic acids in good to high yields.

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