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274-78-2

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274-78-2 Usage

General Description

Imidazo[1,2-c]pyrimidine is a heterocyclic compound with a fused imidazole-pyrimidine ring structure. It is commonly used as a core scaffold in the design and synthesis of various pharmaceuticals and agrochemicals due to its potential biological activities. Imidazo[1,2-c]pyrimidine derivatives have been reported to exhibit a wide range of pharmacological activities, including antiviral, anticancer, antifungal, antihypertensive, and anti-inflammatory properties. These compounds have also been investigated for their potential use in treating neurological disorders and as inhibitors of protein kinases. Due to their diverse biological activities, Imidazo[1,2-c]pyrimidine derivatives hold promise as lead compounds for the development of new therapeutic agents in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 274-78-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,7 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 274-78:
(5*2)+(4*7)+(3*4)+(2*7)+(1*8)=72
72 % 10 = 2
So 274-78-2 is a valid CAS Registry Number.

274-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name imidazo[1,2-c]pyrimidine

1.2 Other means of identification

Product number -
Other names 1,3a,5-Triazaindene

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:274-78-2 SDS

274-78-2Relevant articles and documents

Design, synthesis and dopamine D4 receptor binding activities of new N-heteroaromatic 5/6-ring Mannich bases

Linz, Sabine,Mueller, Joerg,Huebner, Harald,Gmeiner, Peter,Troschuetz, Reinhard

scheme or table, p. 4448 - 4458 (2009/12/04)

A series of phenylpiperazine-methyl-substituted 1H-pyrrolo[2,3-c]pyridine, imidazo[1,2-c]-, pyrrolo[2,3-d]- and pyrrolo[3,2-d]pyrimidines were prepared as selective dopamine D4-ligands. The pyrrolo[2,3-d]pyrimidine derivatives 12d (Ki = 1,9 nM)

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