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3458-56-8

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3458-56-8 Usage

Chemical structure

An imidazo[1,2-a]pyrimidine derivative

Functional groups

Phenyl ring
Methylsulfonyl group attached to the para position of the phenyl ring

Biological activities

Enzyme inhibition: Studied as an inhibitor of certain enzymes
Potential therapeutic applications: Investigated for its potential in treating various diseases

Research significance

Promising candidate for further research and development in medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 3458-56-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,5 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3458-56:
(6*3)+(5*4)+(4*5)+(3*8)+(2*5)+(1*6)=98
98 % 10 = 8
So 3458-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H11N3O2S/c1-19(17,18)11-5-3-10(4-6-11)12-9-16-8-2-7-14-13(16)15-12/h2-9H,1H3

3458-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methylsulfonylphenyl)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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3458-56-8 SDS

3458-56-8Relevant articles and documents

CuI-catalyzed aerobic oxidative α-aminaton cyclization of ketones to access aryl or alkenyl-substituted imidazoheterocycles

Zhang, Yuhong,Zhang, Yuanfei,Chen, Zhengkai,Wu, Wenliang,Su, Weiping

supporting information, p. 12494 - 12504 (2014/01/17)

CuI-catalyzed aerobic oxidative synthesis of imidazoheterocycles has been achieved. Four hydrogen atoms were removed in one step. This protocol was compatible with a broad range of functional groups, and it has been also successfully extended to unsaturated ketones, bringing about the formation of alkenyl-substituted imidazoheterocycles, which were difficult to prepare by previous means. Preliminary mechanistic studies indicated that this reaction was most likely to proceed through a catalytic Ortoleva-King reaction. By using this method, the marketed drug Zolimidine could be prepared with 90% yield on a gram scale from commercially available materials.

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