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33426-53-8

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33426-53-8 Usage

Description

1H-Purine, 8-(methylthio)-, also known as 8-(methylthio)purine, is a chemical compound that belongs to the purine family. It is the methylthio derivative of purine and is commonly found in various plants and microorganisms. 1H-Purine, 8-(methylthio)has potential bioactive properties and is being studied for its potential pharmacological applications, particularly in the field of medicine and drug discovery. Its molecular structure and properties make it a promising candidate for the development of new therapeutic agents. 1H-Purine, 8-(methylthio)is a compound of interest in the scientific community, and ongoing research is being conducted to further understand its potential uses and applications.

Uses

Used in Pharmaceutical Industry:
1H-Purine, 8-(methylthio)is used as a pharmaceutical agent for its potential therapeutic applications. Its bioactive properties make it a promising candidate for the development of new drugs and therapeutic agents, particularly in the field of medicine and drug discovery.
Used in Drug Discovery:
1H-Purine, 8-(methylthio)is used as a compound of interest in drug discovery. Its unique molecular structure and properties make it a valuable candidate for the development of new therapeutic agents, as it may possess novel mechanisms of action or exhibit synergistic effects when combined with other compounds.
Used in Research:
1H-Purine, 8-(methylthio)is used as a subject of research in scientific studies. Ongoing research is being conducted to further understand its potential uses and applications, as well as to explore its bioactive properties and pharmacological effects. This research may lead to the discovery of new therapeutic agents and contribute to the advancement of medicine and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 33426-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,2 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33426-53:
(7*3)+(6*3)+(5*4)+(4*2)+(3*6)+(2*5)+(1*3)=98
98 % 10 = 8
So 33426-53-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N4S/c1-11-6-9-4-2-7-3-8-5(4)10-6/h2-3H,1H3,(H,7,8,9,10)

33426-53-8SDS

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 1H-Purine, 8-(methylthio)-

1.2 Other means of identification

Product number -
Other names 8-Methylthio-purin

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:33426-53-8 SDS

33426-53-8Relevant articles and documents

DEAMINATION, INVOLVING RING OPENING, IN REACTIONS OF 1-AMINOPURINIUM MESITYLENESULFONATES WITH METHANOLIC AMMONIA

Kos, N. J.,Jongejan, H.,van der Plas, H. C.

, p. 4841 - 4848 (2007/10/02)

On reaction of 1-aminopurinium mesitylenesulfonates with methanolic ammonia N-deamination occurs.For 1-amino-, 1-amino-8-(methylthio)-, 1-amino-8-phenyl-, 1-amino-2-methyl-, 1-amino-6-methyl- and 1-amino-8-phenyl-9-methylpurinium mesitylenesulfonate this reaction proceeds for at least 75percent via ring opening as shown by the isolation of 1-15N-labelled purines when 15N-labelled methanolic ammonia was used. 1-Amino-9-methylpurinium mesitylenesulfonate gave N-deamination without ring opening.The reaction of 1-amino-6-(methylthio)purinium mesitylenesulfonate with methanolic ammonia involves, besides deamination, partial substitution of the methylthio group; no ring opening is involved.However, ring opening followed by substitution occurs in the reaction of 1-amino-2-(methylthio)purinium mesitylenesulfonate; the reaction proceeds via an adduct at position 2.

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