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59938-40-8

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59938-40-8 Usage

General Description

3-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde is a chemical compound with the molecular formula C8H5BrN2O. It is a heterocyclic compound containing an imidazole ring fused to a pyridine ring with a bromine atom attached to the imidazole ring and an aldehyde group attached to the pyridine ring. 3-bromoimidazo[1,2-a]pyridine-2-carbaldehyde is commonly used in organic synthesis as a building block in the preparation of various complex molecules and pharmaceutical compounds. It has also been studied for its potential biological activities, including antimicrobial and antitumor properties. Overall, 3-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde is a valuable chemical intermediate with multiple applications in the field of organic chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 59938-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,3 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59938-40:
(7*5)+(6*9)+(5*9)+(4*3)+(3*8)+(2*4)+(1*0)=178
178 % 10 = 8
So 59938-40-8 is a valid CAS Registry Number.

59938-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-bromo-2-formylimidazo[1,2-a]pyridine

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:59938-40-8 SDS

59938-40-8Relevant articles and documents

Synthesis of new substituted imidazo[1,2-a]pyridinylpropenenitriles through sequential one-pot Suzuki–Miyaura/Knoevenagel reactions in aqueous medium

Bakhta, Saléha,Kabri, Youssef,Crozet, Maxime D.,Nedjar-Kolli, Bellara,Vanelle, Patrice

, p. 2561 - 2571 (2019)

A series of imidazo[1,2-a]pyridinylpropenenitriles were synthesized via consecutive one-pot Suzuki–Miyaura and Knoevenagel reactions in water/ethanol mixture between imidazo[1,2-a]pyridine-2-carbaldehydes, arylboronic acids and malononitrile, methyl cyanoacetate or ethyl cyanoacetate. This environmental friendly procedure tolerates a wide range of boronic acids and affords a new substituted imidazo[1,2-a]pyridinyl propenenitriles in good yields under microwave irradiation.

Pyrrolization processes of vinyl substituted imidazo[1,2-a]pyridine, pyrimidine and 1,8-naphthyridine

Chavignon,Teulade,Madesclaire,Gueiffier,Blache,Viols,Chapat,Dauphin

, p. 691 - 697 (2007/10/02)

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