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175724-46-6

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175724-46-6 Usage

General Description

6-Bromo-2-chloro-4-methylquinazoline is a chemical compound with the molecular formula C9H6BrClN2. It is a quinazoline derivative with a bromine atom at the 6th position, a chlorine atom at the 2nd position, and a methyl group at the 4th position. 6-Bromo-2-chloro-4-methylquinazoline has potential applications in the pharmaceutical industry, as quinazolines are known to possess various biological activities, including anticancer, antiviral, and antibacterial properties. Additionally, quinazoline derivatives have been studied for their potential use as kinase inhibitors, which are important in the development of new cancer treatments. Due to its unique structure and potential pharmaceutical applications, 6-Bromo-2-chloro-4-methylquinazoline is a compound of interest for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 175724-46-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,7,2 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 175724-46:
(8*1)+(7*7)+(6*5)+(5*7)+(4*2)+(3*4)+(2*4)+(1*6)=156
156 % 10 = 6
So 175724-46-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H6BrClN2/c1-5-7-4-6(10)2-3-8(7)13-9(11)12-5/h2-4H,1H3

175724-46-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-BROMO-2-CHLORO-4-METHYLQUINAZOLINE

1.2 Other means of identification

Product number -
Other names 6-bromo-2-choro-4-methylquinazoline

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:175724-46-6 SDS

175724-46-6Downstream Products

175724-46-6Relevant articles and documents

Trialkylalanes in palladium-catalyzed chemo- and regioselective alkylations

Mangalagiu, Ionel,Benneche, Tore,Undheim, Kjell

, p. 1309 - 1312 (1996)

Carbosubstitution in halogenoazines with alkyl groups is readily effected under the influence of Pd-catalysis with alanes as the donor of the alkyl group.

CHEMICAL ENTITIES AND THERAPEUTIC USES THEREOF

-

Page/Page column 111; 73, (2009/05/30)

Certain chemical entities that modulate PI3 kinase activity, and chemical entities, pharmaceutical compositions, and methods of treatments of diseases and conditions associated with PB kinase activity are described.

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