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30384-93-1

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30384-93-1 Usage

General Description

2-Methyl-imidazo[1,2-a]pyridine-3-carbaldehyde is a chemical compound with a heterocyclic structure that contains an imidazole and pyridine ring. It is commonly used as a building block in the synthesis of various pharmaceuticals and agricultural chemicals. 2-METHYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE exhibits potential biological activities, including as a protein kinase inhibitor and an anti-viral agent. Its unique structure and reactivity make it a valuable tool in medicinal chemistry research for the development of new drugs. Additionally, 2-Methyl-imidazo[1,2-a]pyridine-3-carbaldehyde is also of interest in the field of organic chemistry for its role in the synthesis of complex organic molecules. Overall, this chemical compound has versatile applications in both the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 30384-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,8 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30384-93:
(7*3)+(6*0)+(5*3)+(4*8)+(3*4)+(2*9)+(1*3)=101
101 % 10 = 1
So 30384-93-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O/c1-7-8(6-12)11-5-3-2-4-9(11)10-7/h2-6H,1H3

30384-93-1SDS

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 2-methylimidazo[1,2-a]pyridine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-Methylimidazo<1,2-a>pyridin-3-carboxaldehyd

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:30384-93-1 SDS

30384-93-1Relevant articles and documents

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Hand et al.

, p. 3377,3379 (1977)

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Aerobic iron(III)-catalyzed direct formylation of imidazo[1,2-a]pyridine using DMSO as carbon source

Xiang, Shijian,Chen, Huoji,Liu, Qiang

supporting information, p. 3870 - 3872 (2016/08/02)

A novel and efficient iron(III)-catalyzed C3-formylation reaction of imidazo[1,2-a]pyridine in an oxygen atmosphere has been developed. The method is conducted in dimethyl sulfoxide (DMSO), which serves as both the carbonyl carbon source and solvent, in the presence of acetic acid to directly generate structurally diverse 3-formylimidazo[1,2-a]pyridine derivatives in moderate to good yields.

Cu-Catalyzed selective C3-formylation of imidazo[1,2-a]pyridine C-H bonds with DMSO using molecular oxygen

Cao, Hua,Lei, Sai,Li, Naiying,Chen, Longbin,Liu, Jingyun,Cai, Huiyin,Qiu, Shuxian,Tan, Jingwen

supporting information, p. 1823 - 1825 (2015/01/30)

Using the widely available DMSO as the formylation reagent under oxidative conditions, an efficient Cu-catalyzed C3-formylation reaction of imidazo[1,2-a]pyridine C-H bonds to directly generate structurally sophisticated 3-formyl imidazo[1,2-a]pyridine derivatives has been developed. The reaction proceeded to generate products in good yields, and used the environmentally friendly molecular oxygen as the oxidant.

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