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90915-18-7

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90915-18-7 Usage

General Description

1H-Benzimidazole-5-carboxylic acid, 1,2-dimethyl-(9CI) is a chemical compound with the molecular formula C10H10N2O2. It is a derivative of benzimidazole and contains a carboxylic acid and two methyl groups. 1H-Benzimidazole-5-carboxylicacid,1,2-dimethyl-(9CI) has potential applications in the pharmaceutical industry, as benzimidazoles are known for their diverse biological activities, including anti-cancer, anti-viral, and anti-inflammatory properties. The presence of a carboxylic acid group also suggests that it may have potential as a building block for the synthesis of other organic compounds. Further research and testing are necessary to fully understand the potential uses and properties of 1H-Benzimidazole-5-carboxylic acid, 1,2-dimethyl-(9CI).

Check Digit Verification of cas no

The CAS Registry Mumber 90915-18-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,9,1 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90915-18:
(7*9)+(6*0)+(5*9)+(4*1)+(3*5)+(2*1)+(1*8)=137
137 % 10 = 7
So 90915-18-7 is a valid CAS Registry Number.

90915-18-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dimethylbenzimidazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1,2-dimethyl-1H-1,3-benzodiazole-5-carboxylic 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:90915-18-7 SDS

90915-18-7Relevant articles and documents

Total synthesis of hypermodified epothilone analogs with potent in vitro antitumor activity

Kuzniewski, Christian N.,Gertsch, Jurg,Wartmann, Markus,Altmann, Karl-Heinz

supporting information; experimental part, p. 1183 - 1186 (2009/04/06)

The convergent total synthesis of hypermodified epothilone analogs 1 and 2 has been achieved with the stereoselective cyclopropanation of allylic alcohol 17 and ring-closing olefin metathesis with diene 22 as the key steps. In spite of significant structural differences between these analogs and the natural epothilone scaffold, 1 and 2 are potent inducers of tubulin polymerization and inhibit the growth of human cancer cells in vitro with sub-nM IC50 values.

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