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Xanthosine, 2-S-[(4-nitrophenyl)methyl]-2-thio-, also known as 4-nitrobenzyl xanthosine-2-thiol, is a chemical compound with the molecular formula C14H12N4O5S2. It is a derivative of xanthosine, a naturally occurring nucleoside, where the 2-amino group is replaced by a 2-thiol group and a 4-nitrobenzyl group is attached to the sulfur atom. Xanthosine, 2-S-[(4-nitrophenyl)methyl]-2-thio- is of interest in chemical and pharmaceutical research due to its potential applications in the synthesis of various biologically active molecules and as a building block for the development of new drugs. Its unique structure allows for the exploration of its properties and reactivity, making it a valuable tool in the field of organic chemistry and medicinal chemistry.

88868-74-0

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88868-74-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88868-74-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,8,6 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88868-74:
(7*8)+(6*8)+(5*8)+(4*6)+(3*8)+(2*7)+(1*4)=210
210 % 10 = 0
So 88868-74-0 is a valid CAS Registry Number.

88868-74-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-((2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-2-(4-nitro-benzylsulfanyl)-1,9-dihydro-purin-6-one

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:88868-74-0 SDS

88868-74-0Upstream product

88868-74-0Relevant academic research and scientific papers

Inhibitors of Inosinic Acid Dehydrogenase. 2-Substituted Inosinic Acids

Wong, Corinne G.,Meyer, Rich B.

, p. 429 - 432 (2007/10/02)

A series of 2-substituted inosine monophosphate (IMP) and inosine derivatives were synthesized and tested for inhibitory activity against IMP dehydrogenase from Escherichia coli.All of the IMP analogues that possessed electron-withdrawing substituents on

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