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Imidazo[1,2-a]pyrimidine, 7-methyl-2-phenyl- is a heterocyclic organic compound with the molecular formula C12H10N4. It is a derivative of imidazo[1,2-a]pyrimidine, which is a tricyclic ring system consisting of an imidazole and a pyrimidine fused together. The compound features a methyl group at the 7th position and a phenyl group at the 2nd position, which are both substituents that can significantly influence its chemical properties and potential applications. Imidazo[1,2-a]pyrimidine, 7-methyl-2-phenyl- is of interest in medicinal chemistry and drug design due to its potential to form stable complexes with various biological targets, such as enzymes and receptors. Its synthesis and study can lead to the development of new therapeutic agents with specific pharmacological activities.

6884-46-4

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6884-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6884-46-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,8 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6884-46:
(6*6)+(5*8)+(4*8)+(3*4)+(2*4)+(1*6)=134
134 % 10 = 4
So 6884-46-4 is a valid CAS Registry Number.

6884-46-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methyl-2-phenylimidazo[1,2-a]pyrimidine

1.2 Other means of identification

Product number -
Other names 7-Methyl-2-phenyl-imidazo<1,2-a>pyrimidin

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:6884-46-4 SDS

6884-46-4Relevant academic research and scientific papers

Synthesis and characterization of novel classes of PDE10A inhibitors - 1H-1,3-benzodiazoles and imidazo[1,2-a]pyrimidines

Moszczyński-P?tkowski, Rafa?,Majer, Jakub,Borkowska, Ma?gorzata,Bojarski, ?ukasz,Janowska, Sylwia,Mat?oka, Miko?aj,Stefaniak, Filip,Smuga, Damian,Bazyd?o, Katarzyna,Dubiel, Krzysztof,Wieczorek, Maciej

, p. 96 - 116 (2018/06/06)

New compounds containing [1,2,4]triazolo [1,5-a]pyridine (I), pyrazolo [1,5-a]pyridine (II), 1H-1,3-benzodiazole (III) and imidazo [1,2-a]pyrimidine (IV) backbones were designed and synthesized for PDE10A interaction. Among these compounds, 1H-1,3-benzodiazoles and imidazo [1,2-a]pyrimidines showed the highest affinity for PDE10A enzyme as well as good metabolic stability. Both classes of compounds were identified as selective and potent PDE10A enzyme inhibitors.

FUSED TRIAZOLE DERIVATIVES AS PHOSPHODIESTERASE 10A INHIBITORS

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Page/Page column 20; 21, (2015/12/08)

Compounds of the general formula (I), wherein one of X1 and X2 represents N, and the other one of X1 and X2 represents -C(CH3), A represents unsubstituted or substituted 5-, 6-or 10-membered aryl or h

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