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2251-78-7

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2251-78-7 Usage

Heterocyclic compound

Contains a benzimidazole ring

Trifluoromethyl group

Enhances biological activity and metabolic stability of drug molecules
Mainly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds
Potential applications in materials science and as a synthetic intermediate in organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 2251-78-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,5 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2251-78:
(6*2)+(5*2)+(4*5)+(3*1)+(2*7)+(1*8)=67
67 % 10 = 7
So 2251-78-7 is a valid CAS Registry Number.

2251-78-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(trifluoromethyl)-1H-benzo[d]imidazol-2(3H)-one

1.2 Other means of identification

Product number -
Other names 4-trifluoromethyl-1,3-dihydro-benzoimidazol-2-one

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:2251-78-7 SDS

2251-78-7Relevant articles and documents

Benzenesulfonamide IDH mutant inhibitor, preparation method and application thereof

-

, (2020/09/23)

The invention discloses a benzenesulfonamide compound represented by a general formula (I) or a pharmaceutically acceptable salt thereof, a preparation method and application thereof. Compared with the prior art, the benzenesulfonamide compound disclosed by the invention can be used as an isocitrate dehydrogenase 2 (IDH2) mutant inhibitor. According to the invention, pharmacological experiment results show that the compound disclosed by the invention has an obvious inhibiting effect on the activity of an IDH2 mutant (mIDH2), can effectively inhibit the process of catalyzing alpha-ketoglutaricacid to generate 2-hydroxyglutaric acid by mIDH2, and can be used for preventing and/or treating various related diseases including cancers and the like caused by IDH2 mutation.

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