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134044-47-6

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134044-47-6 Usage

General Description

2-(3-Bromo-phenyl)-imidazo[1,2-a]pyrimidine is a chemical compound with a molecular formula C11H7BrN4. It is a heterocyclic compound that consists of an imidazo[1,2-a]pyrimidine ring system with a 3-bromo-phenyl substituent. 2-(3-BROMO-PHENYL)-IMIDAZO[1,2-A]PYRIMIDINE is widely used in medicinal chemistry and drug discovery due to its potential pharmacological properties. It has been investigated for its ability to inhibit or modulate specific biological targets, making it a valuable compound in the development of new pharmaceuticals. Additionally, it has also been studied for its potential use in materials science and in the synthesis of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 134044-47-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,0,4 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134044-47:
(8*1)+(7*3)+(6*4)+(5*0)+(4*4)+(3*4)+(2*4)+(1*7)=96
96 % 10 = 6
So 134044-47-6 is a valid CAS Registry Number.

134044-47-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-bromophenyl)imidazo[1,2-a]pyrimidine

1.2 Other means of identification

Product number -
Other names -

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

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More Details:134044-47-6 SDS

134044-47-6Relevant articles and documents

Synthesis and antibacterial activity of some imidazo[1,2-a[pyrimidine derivatives

Rival,Grassy,Michel

, p. 1170 - 1176 (2007/10/02)

A series of 75 imidazo[1,2-a]pyrimidine derivatives were synthesized. The 'in vitro' antibacterial activity of these compounds and their corresponding α-bromoketones against a variety of gram (+), gram (-) bacteria and Mycobacterium species is reported. Some of the prepared derivatives exhibited potent antimicrobial activity.

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