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6-chloro-N-phenylquinazolin-4-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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 academic research and scientific papers

PRODUCTION OF INDUCED PLURIPOTENT STEM CELLS

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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.

POTENT SMALL MOLECULE INHIBITORS OF AUTOPHAGY, AND METHODS OF USE THEREOF

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Page/Page column 54-55, (2011/02/24)

Certain aspects of the invention relates to small molecule autophagy inhibitors, and their use for treatment and prevention of cancers and acute pancreatitis. As disclosed herein, a small molecule inhibitor of autophagy was been identified from an image-based screen in a known bioactive library. It was found that this autophagy inhibitor functions by promoting the degradation of type III PI3 kinase complex which is required for initiating autophagy. Medicinal chemistry studies led to small molecular autophagy inhibitors with improved potency and selectivity.

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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