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59169-66-3

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59169-66-3 Usage

Chemical compound

6-chloro-N-phenylquinazolin-4-amine

Family

Quinazolin-4-amine

Derivative of

Quinazoline (a bicyclic organic compound)

Structure

Contains a chlorine atom and a phenyl group

Potential applications

Medicinal chemistry

Biological activities

May have biological activities and pharmacological properties

Value

Valuable entity for drug discovery and development

Molecular structure

Promising lead compound for design and synthesis of new pharmaceuticals

Ongoing research

Exploration of potential therapeutic applications and elucidation of chemical properties and biological effects.

Check Digit Verification of cas no

The CAS Registry Mumber 59169-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,6 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59169-66:
(7*5)+(6*9)+(5*1)+(4*6)+(3*9)+(2*6)+(1*6)=163
163 % 10 = 3
So 59169-66-3 is a valid CAS Registry Number.

59169-66-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-N-phenylquinazolin-4-amine

1.2 Other means of identification

Product number -
Other names (6-chloro-quinazolin-4-yl)-phenyl-amine

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:59169-66-3 SDS

59169-66-3Downstream Products

59169-66-3Relevant articles and documents

PRODUCTION OF INDUCED PLURIPOTENT STEM CELLS

-

Page/Page column 60-61, (2012/06/30)

The present disclosure relates to methods and compositions that improve the in vitro production of induced pluripotent stem cells through the use of compounds that promote degradation of p53. The disclosure also relates to compositions and methods for the treatment of cancer, pancreatitis and intracellular pathogens.

Discovery and SAR of 6-substituted-4-anilinoquinazolines as non-competitive antagonists of mGlu5

Felts, Andrew S.,Saleh, Sam A.,Le, Uyen,Rodriguez, Alice L.,Weaver, C. David,Conn, P. Jeffrey,Lindsley, Craig W.,Emmitte, Kyle A.

scheme or table, p. 6623 - 6626 (2010/06/12)

A high-throughput cell-based screen identified a series of 6-substituted-4-anilinoquinazolines as non-competitive antagonists of metabotropic glutamate receptor 5 (mGlu5). This Letter describes the SAR of this series and the profile of selected

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