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8-Chloro-2-methyl-imidazo[1,2-a]pyridine-3-carboxylic acid ethyl ester is a chemical compound with a molecular formula of C11H9ClN2O2. It is a derivative of imidazo[1,2-a]pyridine, a heterocyclic compound commonly used in medicinal chemistry. This particular chemical is an ethyl ester, which means it is an ester of 8-Chloro-2-methyl-imidazo[1,2-a]pyridine-3-carboxylic acid and ethanol. Ethyl esters are often used as solvents, and 8-CHLORO-2-METHYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER may also have potential pharmaceutical or biological applications. Its specific properties and uses would depend on the specific nature and behavior of the compound in a given context, but it is likely to be of interest to researchers and companies working in the pharmaceutical, chemical, or biotechnology industries.

885276-29-9

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885276-29-9 Usage

Uses

Used in Pharmaceutical Industry:
8-Chloro-2-methyl-imidazo[1,2-a]pyridine-3-carboxylic acid ethyl ester is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a promising candidate for the development of new drugs with potential therapeutic applications.
Used in Chemical Industry:
In the chemical industry, 8-Chloro-2-methyl-imidazo[1,2-a]pyridine-3-carboxylic acid ethyl ester is used as a solvent for various chemical reactions. Its ability to dissolve a wide range of substances makes it a valuable component in the synthesis of other chemicals and materials.
Used in Biotechnology Industry:
8-Chloro-2-methyl-imidazo[1,2-a]pyridine-3-carboxylic acid ethyl ester may also have potential applications in the biotechnology industry. Its unique structure and properties could be utilized in the development of new biotechnological processes or products, such as in the synthesis of bioactive compounds or as a component in drug delivery systems.

Check Digit Verification of cas no

The CAS Registry Mumber 885276-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 885276-29:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*6)+(2*2)+(1*9)=219
219 % 10 = 9
So 885276-29-9 is a valid CAS Registry Number.

885276-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 8-chloro-2-methylimidazo[1,2-a]pyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names 8-CHLORO-2-METHYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER

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:885276-29-9 SDS

885276-29-9Downstream Products

885276-29-9Relevant academic research and scientific papers

Design, synthesis and biological activity of N-(2-phenoxy)ethyl imidazo[1,2-a]pyridine-3-carboxamides as new antitubercular agents

Wang, Apeng,Lv, Kai,Li, Linhu,Liu, Hongtao,Tao, Zeyu,Wang, Bin,Liu, Mingliang,Ma, Chao,Ma, Xican,Han, Bing,Wang, Aoyu,Lu, Yu

, p. 715 - 725 (2019/06/24)

A series of N-(2-phenoxy)ethyl imidazo[1,2-a]pyridine-3-carboxamides (IPAs), based on the structure of WZY02 discovered in our lab, were designed and synthesized as new anti-TB agents. Results reveal that many of them exhibit excellent in vitro inhibitory activity with low nanomolar MIC values against both drug-sensitive MTB strain H37Rv and drug-resistant clinical isolates. Compounds 15b and 15d display good safety and pharmacokinetic profiles, suggesting their promising potential to be lead compounds for future antitubercular drug discovery.

Microwave assisted synthesis of disubstituted imidazo[1,2-a]pyridine-3-carboxylic acid esters

Li, Lin-Hu,Wu, Zhao-Yang,Li, Zhuo-Rong,Liu, Ming-Liang,Guo, Hui-Yuan,Zhang, Qiu-Rong

, p. 2087 - 2096 (2015/12/12)

A novel and efficient synthetic method leveraging microwave-assisted organic synthesis (MAOS) to prepare disubstituted imidazo[1,2-a]- pyridine-3-carboxylic acid esters (IPCEs) (3a-z), the key intermediates for a class of novel anti-tuberculosis agents, is reported. Under microwave heating at 120 °C for 20 or 30 min, the condensations of 2-aminopyridines (1a-k) and ethyl 2-halogenated acetoacetates (2a-d) were conveniently performed in ethanol with acceptable yields.

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