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5417-86-7

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5417-86-7 Usage

General Description

6-N-PROPOXYPURINE is a chemical compound that belongs to the purine class and is derived from the nucleotide adenosine. It is a potent adenosine receptor antagonist with potential application in the treatment of cognitive impairment and neurodegenerative disorders. It acts as a stimulant of the central nervous system and has been shown to improve cognitive function in animal models. 6-N-PROPOXYPURINE may also have potential as a therapeutic agent for conditions such as Alzheimer's disease and Parkinson's disease, although further research is needed to determine its efficacy and safety in humans.

Check Digit Verification of cas no

The CAS Registry Mumber 5417-86-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5417-86:
(6*5)+(5*4)+(4*1)+(3*7)+(2*8)+(1*6)=97
97 % 10 = 7
So 5417-86-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N4O/c1-2-3-13-8-6-7(10-4-9-6)11-5-12-8/h4-6H,2-3H2,1H3

5417-86-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-N-PROPOXYPURINE

1.2 Other means of identification

Product number -
Other names 6-Propyloxy-1H-purine

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:5417-86-7 SDS

5417-86-7Downstream Products

5417-86-7Relevant articles and documents

Simple, chemoselective hydrogenation with thermodynamic stereocontrol

Iwasaki, Kotaro,Wan, Kanny K.,Oppedisano, Alberto,Crossley, Steven W. M.,Shenvi, Ryan A.

, p. 1300 - 1303 (2014/02/14)

Few methods permit the hydrogenation of alkenes to a thermodynamically favored configuration when steric effects dictate the alternative trajectory of hydrogen delivery. Dissolving metal reduction achieves this control, but with extremely low functional group tolerance. Here we demonstrate a catalytic hydrogenation of alkenes that affords the thermodynamic alkane products with remarkably broad functional group compatibility and rapid reaction rates at standard temperature and pressure.

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