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131747-42-7

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131747-42-7 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 131747-42-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,7,4 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 131747-42:
(8*1)+(7*3)+(6*1)+(5*7)+(4*4)+(3*7)+(2*4)+(1*2)=117
117 % 10 = 7
So 131747-42-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H4F3NO/c8-7(9,10)5-2-1-3-11-6(5)4-12/h1-4H

131747-42-7 Well-known Company Product Price

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  • TCI America

  • (T3270)  6-(Trifluoromethyl)-2-pyridinecarboxylic Acid  >98.0%(GC)(T)

  • 131747-42-7

  • 1g

  • 1,580.00CNY

  • Detail
  • Alfa Aesar

  • (H63138)  6-(Trifluoromethyl)pyridine-2-carboxylic acid, 98%   

  • 131747-42-7

  • 250mg

  • 267.0CNY

  • Detail
  • Alfa Aesar

  • (H63138)  6-(Trifluoromethyl)pyridine-2-carboxylic acid, 98%   

  • 131747-42-7

  • 1g

  • 904.0CNY

  • Detail

131747-42-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Trifluoromethyl-6-Pyridinecarboxylic Acid

1.2 Other means of identification

Product number -
Other names 6-(Trifluoromethyl)picolinic acid

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:131747-42-7 SDS

131747-42-7Relevant articles and documents

Photoinduced FeCl3-Catalyzed Alkyl Aromatics Oxidation toward Degradation of Polystyrene at Room Temperature?

Zhang, Guoxiang,Zhang, Zongnan,Zeng, Rong

supporting information, p. 3225 - 3230 (2021/09/28)

While polystyrene is widely used in daily life as a synthetic plastic, the subsequently selective degradation is still very challenging and highly required. Herein, we disclose a highly practical and selective reaction for the catalytically efficient oxidation of alkyl aromatics (including 1°, 2°, and 3° alkyl aromatics) to carboxylic acids. While dioxygen was used as the sole terminal oxidant, this protocol was catalyzed by the inexpensive and readily available ferric compound (FeCl3) with irradiation of visible light (blue LEDs) under only 1 atmosphere of O2 at room temperature. This system could further facilitate the selective degradation of polystyrene to benzoic acid, providing an important and practical tool to generate high-value chemical from abundant polystyrene wastes.

Compound with IDH mutant inhibitory activity, preparation method and application thereof

-

Paragraph 0037; 0041-0043, (2020/09/23)

The invention belongs to the field of medicines, and particularly relates to a s-triazine compound with structural characteristics of a general formula I or a pharmaceutically acceptable salt thereof,a pharmaceutical composition and a preparation method thereof, and application of the s-triazine compound or the pharmaceutically acceptable salt and the pharmaceutical composition in preparation ofIDH2 mutant inhibitors. According to the invention, pharmacological experiment results show that the compound disclosed by the invention has an obvious inhibition effect on the activity of an IDH2 mutant (mIDH2), can effectively inhibit the process that alpha-ketoglutaric acid is catalyzed by mIDH2 to generate 2-hydroxyglutaric acid, and can be used for preparing drugs for preventing and/or treating various related diseases caused by IDH2 mutation, wherein the diseases comprise cancers carrying IDH2 mutation.

COMBINATION THERAPY FOR TREATING MALIGNANCIES

-

Paragraph 0343, (2018/11/21)

Provided are methods and compositions for treating AML in patients carrying an IDH2 mutation using a combination of an inhibitor of a mutant IDH2 enzyme and an AML induction and consolidation therapy.

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