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159589-71-6

159589-71-6

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159589-71-6 Usage

General Description

2-(2-Methyl-1H-imidazol-1-yl)benzoic acid is a chemical compound with the molecular formula C11H10N2O2. It is a derivative of benzoic acid and contains an imidazole ring. 2-(2-Methyl-1H-imidazol-1-yl)benzoic acid is often used in the pharmaceutical industry, particularly in the synthesis of drugs that target the imidazoline receptor. It has also been studied for its potential use in the treatment of various medical conditions, including neurological disorders and cardiovascular diseases. Additionally, 2-(2-Methyl-1H-imidazol-1-yl)benzoic acid has been used as a building block in the development of new organic molecules with potential biological activity. Overall, this chemical compound has shown promising applications in medicine and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 159589-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,5,8 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 159589-71:
(8*1)+(7*5)+(6*9)+(5*5)+(4*8)+(3*9)+(2*7)+(1*1)=196
196 % 10 = 6
So 159589-71-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2O2/c1-8-12-6-7-13(8)10-5-3-2-4-9(10)11(14)15/h2-7H,1H3,(H,14,15)

159589-71-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methylimidazol-1-yl)benzoic acid

1.2 Other means of identification

Product number -
Other names 2-(2-Methyl-1H-imidazol-1-yl)benzoic 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:159589-71-6 SDS

159589-71-6Downstream Products

159589-71-6Relevant articles and documents

Preparation of highly potent and selective non-peptide antagonists of the arginine vasopressin V1A receptor by introduction of a 2-ethyl-1H-1-imidazolyl group

Shimada, Yoshiaki,Akane, Hiroaki,Taniguchi, Nobuaki,Matsuhisa, Akira,Kawano, Noriyuki,Kikuchi, Kazumi,Yatsu, Takeyuki,Tahara, Atsuo,Tomura, Yuichi,Kusayama, Toshiyuki,Wada, Koh-Ichi,Tsukada, Junko,Tsunoda, Takashi,Tanaka, Akihiro

, p. 764 - 769 (2007/10/03)

To find a new series of arginine vasopressin (AVP) V1A receptor antagonists, the influence of the 2-phenyl group of 2-phenyl-4′-[(2,3,4,5- tetrahydro-1H-1-benzazepin-1-yl)carbonyl]benzanilide (7) was investigated. Replacement of the 2-phenyl group by a 2-ethyl-1H-imidazol-1-yl group was effective in yielding a V1A-selective compound. Moreover, this imidazolyl group was introduced in the same position in YM-35471 (6), and further studies of these compounds were performed. Consequently, we found that the (Z)-4′-({4,4-difluoro-5-[(N-cyclo-propylcarbamoyl) methylene]-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl}carbonyl)-2-(2-ethyl-1H-1- imidazol-1-yl)benzanilide (9f) exhibited highly potent affinity and selectivity, and was the most potent antagonist for the V1A receptor among our compounds. The synthesis and pharmacological evaluation of these compounds are described in this paper

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