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2-Chloro-8-methoxyquinazoline is a quinazoline derivative characterized by the presence of a chlorine atom at the 2nd position and a methoxy group at the 8th position. This chemical compound is known for its potential biological activities and has been the subject of pharmacological studies due to its diverse biological properties and potential therapeutic applications.

944060-66-6

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944060-66-6 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Chloro-8-methoxyquinazoline serves as a building block in the synthesis of various pharmaceutical compounds and chemical intermediates. Its unique structure and functional groups contribute to the development of new drugs with improved therapeutic properties.
Used in Medical Research:
In the field of medical research, 2-chloro-8-methoxyquinazoline is utilized for its potential applications in drug development. Its pharmacological properties are being investigated to explore its efficacy in treating various diseases and conditions.
Used in Drug Development:
Due to its diverse biological properties, 2-chloro-8-methoxyquinazoline is considered a promising candidate for drug development. Researchers are actively studying its potential therapeutic applications to identify new treatment options for various health issues.

Check Digit Verification of cas no

The CAS Registry Mumber 944060-66-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,0,6 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 944060-66:
(8*9)+(7*4)+(6*4)+(5*0)+(4*6)+(3*0)+(2*6)+(1*6)=166
166 % 10 = 6
So 944060-66-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H7ClN2O/c1-13-7-4-2-3-6-5-11-9(10)12-8(6)7/h2-5H,1H3

944060-66-6SDS

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 2-chloro-8-methoxyquinazoline

1.2 Other means of identification

Product number -
Other names 2-chloro-8-methoxy-quinazoline

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:944060-66-6 SDS

944060-66-6Relevant academic research and scientific papers

Synthesis and biological studies of new quinazolines with ether functions in position 2

Brahmaiah, Dabbugoddu,Bhavani, Anagani Kanaka Durga,Aparna, Pasula,Kumar, Nangunoori Sampath,Solhi, Hélène,Le Guevel, Rémy,Baratte, Blandine,Ruchaud, Sandrine,Bach, Stéphane,Mosset, Paul,Grée, René

, p. 96 - 107 (2019/05/15)

A series of new quinazolines linked to triazoles through an ether chain in position 2 has been designed and synthetized through a flexible route. Cytotoxicity assays on selected cancer cell lines and inhibition studies toward a panel of representative mam

QUINAZOLINES FOR PDK1 INHIBITION

-

, (2008/06/13)

The invention provides novel quinazoline compounds that are inhibitors of PDK1. Also provided are pharmaceutical compositions including the compounds, and methods of treating proliferative diseases, such as cancers, with the compounds or compositions.

NEUROLOGICALLY-ACTIVE COMPOUNDS

-

Page 40; 53, (2010/02/06)

The present invention relates to neurologically-active compounds, being heterocyclic compounds having two fused 6-membered rings with a nitrogen atom at position 1 and a hydroxy or mercapto group at position 8 with at least one ring being aromatic. Also disclosed are processes for the preparation of these compounds and their use as pharmaceutical or veterinary agents, in particular for the treatment of neurological conditions, more specifically neurodegenerative conditions such as Alzheimer's disease.

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