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6-chloro-2-methyl-3-(pyrimidin-2-yl)quinazolin-4(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37905-56-9

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37905-56-9 Usage

Chemical Class

Quinazoline

Core Structure

Quinazoline

Substituents

Chlorine atom at position 6
Methyl group at position 2
Pyrimidine ring at position 3

Potential Pharmacological Properties

Specific pharmacological properties yet to be fully elucidated

Applications

Potential interest in drug development

Further Research

Specific uses and applications require additional investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 37905-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,0 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 37905-56:
(7*3)+(6*7)+(5*9)+(4*0)+(3*5)+(2*5)+(1*6)=139
139 % 10 = 9
So 37905-56-9 is a valid CAS Registry Number.

37905-56-9SDS

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 6-chloro-2-methyl-3-pyrimidin-2-ylquinazolin-4-one

1.2 Other means of identification

Product number -
Other names 6-chloro-2-methyl-3-(pyrimidin-2-yl)quinazolin-4(3H)-one

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:37905-56-9 SDS

37905-56-9Downstream Products

37905-56-9Relevant academic research and scientific papers

Synthesis and antileukemic activity of new 3-(5-methylisoxazol-3-yl) and 3-(pyrimidin-2-yl)-2-styrylquinazolin-4(3H)-ones

Raffa, Demetrio,Daidone, Giuseppe,Maggio, Benedetta,Cascioferro, Stella,Plescia, Fabiana,Schillaci, Domenico

, p. 451 - 455 (2004)

3-(3-Methylisoxazol-5-yl) and 3-(pyrimidin-2-yl)-2-styrylquinazolin-4(3H)- ones 8a-l and 9a,c-e,h-l were synthesized by refluxing in acetic acid the corresponding 2-methylquinazolinones 6 and 8 with the opportune benzoic aldehyde for 12 h. The synthesized styrylquinazolinones 8a-l and 9a,c-e,h-l were tested in vitro for their antileukemic activity against L-1210 (murine leukemia), K-562 (human chronic myelogenous leukemia) and HL-60 (human leukemia) cell lines showing in some cases good activity.

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