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"9-(2-deoxypentofuranosyl)-6-[(1-methyl-4-nitro-1H-imidazol-5-yl)selanyl]-9H-purin-2-amine" is a complex organic compound with a molecular formula of C15H15N7O5Se. 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 2-deoxypentofuranosyl group attached to the 9-position of the purine ring, and a selenoether linkage connecting a 1-methyl-4-nitro-1H-imidazol-5-yl group to the 6-position. The presence of a nitro group and a selenium atom in the molecule contribute to its unique chemical properties and potential applications in various fields, such as pharmaceuticals and materials science.

52192-42-4

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52192-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52192-42-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,9 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52192-42:
(7*5)+(6*2)+(5*1)+(4*9)+(3*2)+(2*4)+(1*2)=104
104 % 10 = 4
So 52192-42-4 is a valid CAS Registry Number.

52192-42-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[2-amino-6-(3-methyl-5-nitroimidazol-4-yl)selanylpurin-9-yl]-2-(hydroxymethyl)oxolan-3-ol

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

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More Details:52192-42-4 SDS

52192-42-4Upstream product

52192-42-4Downstream Products

52192-42-4Relevant academic research and scientific papers

α- and β-2'-Deoxy-6-R-substituted selenoguanosine compounds

-

, (2008/06/13)

Treatment of the α and β anomers of 2'-deoxy-6-selenoguanosine with alkyl halides, p-nitrobenzyl bromide, and 5-chloro-1-methyl-4-nitroimidazole under basic conditions has produced the desired products, which are 2'-deoxy-6-R-selenoguanosines where R is the substituent group [2-amino-6-R-seleno-9-(2-deoxy-α- and β-D-erythro-pentofuranosyl)purines] and R is preferably lower alkyl or aryl. The animal test screening indicated substantial activity for several members of this group of compounds against mouse leukemia L-1210.

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