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1H-Benzimidazole-2-carboxylic acid,4-methyl-(9CI) is a chemical compound with the molecular formula C10H8N2O2. It is a derivative of benzimidazole, a heterocyclic aromatic organic compound. The 4-methyl substitution on the benzimidazole ring endows 1H-Benzimidazole-2-carboxylicacid,4-methyl-(9CI) with unique properties and potential applications.
Used in Pharmaceutical Industry:
1H-Benzimidazole-2-carboxylic acid,4-methyl-(9CI) is used as a building block for the development of new drugs due to its unique chemical structure and potential biological activity.
Used in Medicinal Chemistry Research:
1H-Benzimidazole-2-carboxylic acid,4-methyl-(9CI) is used as a research compound to study its interactions with biological targets and explore its potential as a therapeutic agent.
Used in Agrochemicals Industry:
1H-Benzimidazole-2-carboxylic acid,4-methyl-(9CI) may have applications in the development of agrochemicals, such as pesticides or herbicides, due to its unique chemical properties.
Used in Materials Science:
1H-Benzimidazole-2-carboxylic acid,4-methyl-(9CI) may also have potential uses in materials science, such as in the development of new materials with specific properties, although further research is needed to fully understand its potential in this field.

673487-32-6

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673487-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 673487-32-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,3,4,8 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 673487-32:
(8*6)+(7*7)+(6*3)+(5*4)+(4*8)+(3*7)+(2*3)+(1*2)=196
196 % 10 = 6
So 673487-32-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O2/c1-5-3-2-4-6-7(5)11-8(10-6)9(12)13/h2-4H,1H3,(H,10,11)(H,12,13)

673487-32-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methyl-1H-benzimidazole-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-Methyl-1H-Benzimidazole-2-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:673487-32-6 SDS

673487-32-6Downstream Products

673487-32-6Relevant academic research and scientific papers

NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS

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Page/Page column 138, (2011/12/02)

Unsaturated nitrogen heterocyclic compounds of formula (I): (I), as defined in the specification, compositions containing them, and processes for preparing such compounds. Provided herein also are methods of treating disorders or diseases treatable by inhibition of PDE10, such as obesity, Huntington's Disease, non-insulin dependent diabetes, schizophrenia, bipolar disorder, obsessive-compulsive disorder, and the like.

BENZIMIDAZOLE CARBOXAMIDES AS RAF KINASE INHIBITORS

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Page/Page column 135, (2008/06/13)

The present invention relates to benzimidazole carboxamides of formula (I), the use of the compounds of formula (I) as inhibitors of as inhibitors of one or more kinases, the use of the compounds of formula (I) for the manufacture of a pharmaceutical composition and a method of treatment, comprising administering said pharmaceutical composition to a patient. Accordingly, the compound of Formula (I) or a pharmaceutically acceptable salt thereof is administered for the treatment of diseases mediated by one or more kinase phathways, preferably by the raf kinase pathway, especially cancers.

HETEROCYCLIC COMPOUNDS

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Page/Page column 33-34, (2008/06/13)

Certain thienopyrrolyl and furanopyrrolyl compounds are disclosed as useful to treat or prevent disorders and conditions mediated by the histamine H4 receptor, including allergic rhinitis.

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