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147700-34-3

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147700-34-3 Usage

Chemical class

Purine derivatives

Structure

Contains a purine core with two methyl groups at the 1 and 3 positions

Substituent

A trimethoxyphenyl group attached to the 8 position

Linker

An ethenyl linker connects the trimethoxyphenyl group to the 8 position

Stereochemistry

The ethenyl linker has an (E)-configuration

Potential applications

Pharmaceutical applications due to its unique chemical structure

Biological activities

May have potential biological activities, but further studies are needed

Pharmacological properties

Specific pharmacological properties are yet to be determined

Applications in medicine

Potential applications in medicine and drug development, but further research is required

Synthetic molecule

It is a synthetically created molecule

Check Digit Verification of cas no

The CAS Registry Mumber 147700-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,7,0 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 147700-34:
(8*1)+(7*4)+(6*7)+(5*7)+(4*0)+(3*0)+(2*3)+(1*4)=123
123 % 10 = 3
So 147700-34-3 is a valid CAS Registry Number.

147700-34-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dimethyl-8-[(E)-2-(3,4,5-trimethoxyphenyl)ethenyl]-7H-purine-2,6-dione

1.2 Other means of identification

Product number -
Other names -

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:147700-34-3 SDS

147700-34-3Relevant articles and documents

Structure-activity relationships of 8-styrylxanthines as A2-selective adenosine antagonists

Jacobson,Gallo-Rodriguez,Melman,Fischer,Maillard,Van Bergen,Van Galen,Karton

, p. 1333 - 1342 (2007/10/02)

A series of substituted 8-styryl derivatives of 1,3,7-alkylxanthines was synthesized as potential A2-selective adenosine receptor antagonists, and the potency at rat brain A1- and A2-receptors was studied in radioligand bi

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