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3-PHENYL-IMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER is a chemical compound that belongs to the class of imidazo[1,2-a]pyridine derivatives. It is characterized by a phenyl group attached to an imidazo[1,2-a]pyridine ring, along with a carboxylic acid and a methyl ester functional group. 3-PHENYL-IMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER is commonly used in pharmaceutical research and drug development due to its potential biological activities, including anti-inflammatory, anti-cancer, and anti-bacterial properties.

132525-00-9

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132525-00-9 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
3-PHENYL-IMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER is used as a research compound for exploring its potential biological activities and therapeutic applications. Its unique molecular structure and functional groups make it a promising candidate for the development of new drugs targeting various diseases and conditions.
Used in Anti-inflammatory Applications:
In the field of medicine, 3-PHENYL-IMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER is used as an anti-inflammatory agent. Its potential to modulate inflammatory pathways and reduce inflammation makes it a valuable tool in the treatment of various inflammatory disorders.
Used in Anti-cancer Applications:
3-PHENYL-IMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER is also used as an anti-cancer agent. Its potential to inhibit cancer cell growth and proliferation, as well as its ability to target specific molecular pathways involved in cancer development, make it a promising candidate for cancer therapy.
Used in Anti-bacterial Applications:
In the field of microbiology, 3-PHENYL-IMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER is used as an anti-bacterial agent. Its potential to inhibit bacterial growth and combat antibiotic-resistant strains highlights its importance in the development of new antimicrobial drugs.
Further research and studies are ongoing to explore the potential applications of 3-PHENYL-IMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER in various fields of medicine and pharmacology, with the aim of harnessing its biological activities for the development of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 132525-00-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,2 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132525-00:
(8*1)+(7*3)+(6*2)+(5*5)+(4*2)+(3*5)+(2*0)+(1*0)=89
89 % 10 = 9
So 132525-00-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H12N2O2/c1-19-15(18)13-14(11-7-3-2-4-8-11)17-10-6-5-9-12(17)16-13/h2-10H,1H3

132525-00-9SDS

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 methyl 3-phenylimidazo[1,2-a]pyridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names Imidazo[1,2-a]pyridine-2-carboxylic acid,3-phenyl-,methylester

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:132525-00-9 SDS

132525-00-9Downstream Products

132525-00-9Relevant academic research and scientific papers

REACTIONS OF ESTERS OF 3-PHENYL-3-CHLORO-2-OXOPROPIONIC ACID WITH 2-AMINOPYRIDINES AND 2-AMINOQUINOLINE

Mamedov, V. A.,Nuretdinov, I. A.,Sibgatullina, F. G.

, p. 2380 - 2382 (2007/10/02)

The reaction of esters of 3-phenyl-3-chloro-2-oxopropionic acid with 2-aminopyridines and 2-aminoquinoline in chloroform at reflux gave derivatives of imidazopyridine and imidazoquinoline in high yield.

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