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3-(6-sulfanylidene-3H-purin-9-yl)propanoic acid is a chemical compound with the molecular formula C8H7N4O3S. It is a derivative of purine, a heterocyclic aromatic organic compound consisting of a pyrimidine ring fused to an imidazole ring. This specific compound features a 3-hydroxypropanoic acid side chain attached to the purine ring, with a sulfur atom (sulfanylidene) bridging the 6-position of the purine and the 3-position of the propanoic acid. The presence of the sulfur atom and the carboxylic acid group give 3-(6-sulfanylidene-3H-purin-9-yl)propanoic acid unique chemical properties and potential applications in various fields, such as pharmaceuticals and biochemistry.

4367-64-0

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4367-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4367-64-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4367-64:
(6*4)+(5*3)+(4*6)+(3*7)+(2*6)+(1*4)=100
100 % 10 = 0
So 4367-64-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N4O2S/c13-5(14)1-2-12-4-11-6-7(12)9-3-10-8(6)15/h3-4H,1-2H2,(H,13,14)(H,9,10,15)

4367-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(6-sulfanylidene-3H-purin-9-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names 6-Mercapto-9H-purin-9-ylpropionsaeure

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

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More Details:4367-64-0 SDS

4367-64-0Downstream Products

4367-64-0Relevant academic research and scientific papers

HYDROLYTIC CLEAVAGE OF 6-OXOPURINES AFTER INTRAMOLECULAR ACYLATION AT N-3

Rosemeyer, Helmut,Seela, Frank

, p. 2669 - 2676 (2007/10/02)

Reaction of 9H-hypoxanthin-9-yl propionic acid (2c) as well as of its 6-mercapto analogue (2d) with N--N'-ethylcarbodiimide hydrochloride results in an intramolecular acylation at N-3 followed by a spontaneous hydroxylation at C-2 and opening of the pyrimidine ring.The products of these reaction sequences are the imidazopyrimidines (5c,d) which were deformylated to give the compounds 6a,b.The half-life values of the ring transformations of 2c,d as well as of its isosteres 2a,b imply that the "over-all" kinetics are 1. independent of the structure of the five-membered ring and 2. strongly effected by the 6-substituent.It is proposed that the intramolecular acylation is the rate-limiting step of the reaction cascade.

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