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3-Nitro-1-pentofuranosyl-1H-1,2,4-triazole is a complex organic compound with the molecular formula C8H9N5O5. It is a derivative of 1,2,4-triazole, a five-membered heterocyclic ring containing three nitrogen atoms, and is fused with a pentofuranosyl group, which is a five-carbon sugar structure. 3-nitro-1-pentofuranosyl-1H-1,2,4-triazole is characterized by the presence of a nitro group (-NO2) attached to the 3-position of the triazole ring. It is synthesized through chemical reactions and is of interest in the field of organic chemistry, potentially for its reactivity or as a building block in the synthesis of more complex molecules. The compound's properties, such as solubility and stability, can be influenced by the presence of the nitro group and the sugar moiety, making it a subject of study for its potential applications in various chemical and pharmaceutical contexts.

24806-95-9

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24806-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24806-95-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,0 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24806-95:
(7*2)+(6*4)+(5*8)+(4*0)+(3*6)+(2*9)+(1*5)=119
119 % 10 = 9
So 24806-95-9 is a valid CAS Registry Number.

24806-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-nitro-1-(β-D-ribofuranosyl)-1,2,4-triazole

1.2 Other means of identification

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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

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More Details:24806-95-9 SDS

24806-95-9Relevant academic research and scientific papers

Structural effects on the phosphorylation of 3-substituted 1-β-d-ribofuranosyl-1,2,4-triazoles by human adenosine kinase

Kumarapperuma, Sidath C.,Sun, Yanjie,Jeselnik, Marjan,Chung, Kiwon,Parker, William B.,Jonsson, Colleen B.,Arterburn, Jeffrey B.

, p. 3203 - 3207 (2007)

The conversion of ribavirin to the monophosphate by adenosine kinase is the rate-limiting step in activation of this broad spectrum antiviral drug. Variation of the 3-substituents in a series of bioisosteric and homologated 1-β-d-ribofuranosyl-1,2,4-triazoles has marked effects on activity with the human adenosine kinase, and analysis of computational descriptors and binding models offers insight for the design of novel substrates.

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