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2-(2-amino-6-chloro-9H-purin-9-yl)-1,4-anhydro-2,3-dideoxy-1-thio-L-threo-pentitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

142941-60-4

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142941-60-4 Usage

Structure

A chemical compound consisting of a purine base connected to a sugar-like molecule and a thiol group.

Potential applications

Due to its purine structure, the compound has potential pharmaceutical applications, such as in antiviral or antitumor drugs.

Biological significance

The purine structure is found in important biological molecules such as DNA and RNA, making the compound a potential candidate for studying the interactions of purine-based molecules with other biological systems.

Antioxidant properties

The presence of the thiol group suggests that the compound may have antioxidant properties.

Additional research needed

Further research and testing are required to fully understand the potential uses and effects of 2-(2-amino-6-chloro-9H-purin-9-yl)-1,4-anhydro-2,3-dideoxy-1-thio-L-threo-pentitol.

Check Digit Verification of cas no

The CAS Registry Mumber 142941-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,9,4 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 142941-60:
(8*1)+(7*4)+(6*2)+(5*9)+(4*4)+(3*1)+(2*6)+(1*0)=124
124 % 10 = 4
So 142941-60-4 is a valid CAS Registry Number.

142941-60-4SDS

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 [(2R,4R)-4-(2-amino-6-chloropurin-9-yl)thiolan-2-yl]methanol

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:142941-60-4 SDS

142941-60-4Downstream Products

142941-60-4Relevant academic research and scientific papers

Enantiospecific Synthesis of 3'-Hetero-dideoxy Nucleoside Analogues as Potential Anti-HIV Agents

Jones, Martin F.,Noble, Stewart A.,Robertson, Colin A.,Storer, Richard,Highcock, Rona M.,Lamont, R. Brian

, p. 1427 - 1436 (2007/10/02)

Two series of analogues of 2',3'-dideoxy carbocyclic nucleosides, in which the 3'-carbon atom is replaced by either an oxygen or a sulfur atom, have been prepared enantiospecifically from diacetone-L-glucose and diacetone-D-glucose respectively.Within eac

TETRAHYDROTHIOPHENE NUCLEOSIDES AS POTENTIAL ANTI-HIV AGENTS

Jones, Martin F.,Noble, Stewart A.,Robertson, Colin A.,Storer, Richard

, p. 247 - 250 (2007/10/02)

A series of novel tetrahydrothiophene nucleosides have been prepared in homochiral form from D-glucose and assessed as anti-HIV agents in whole cell assay.

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