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2-chloro-9-pentofuranosyl-9H-purine, also known as 2-chloro-9-(2-deoxy-β-D-ribofuranosyl)-9H-purine, is a chemical compound that belongs to the purine family. It is a derivative of guanine, a naturally occurring purine base found in DNA and RNA, with a chlorine atom attached at the 2-position and a 2-deoxy-β-D-ribofuranosyl group at the 9-position. 2-chloro-9-pentofuranosyl-9H-purine is of interest in the field of medicinal chemistry and nucleoside chemistry, as it may exhibit unique biological properties or serve as a building block for the synthesis of more complex molecules. The presence of the chlorine atom and the modified sugar moiety can potentially alter the compound's reactivity, stability, and interactions with enzymes and other biomolecules, making it a subject of study for potential therapeutic applications or as a probe to understand the structure-activity relationships of purine-based compounds.

5466-11-5

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5466-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5466-11-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5466-11:
(6*5)+(5*4)+(4*6)+(3*6)+(2*1)+(1*1)=95
95 % 10 = 5
So 5466-11-5 is a valid CAS Registry Number.

5466-11-5SDS

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 2-(2-chloropurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol

1.2 Other means of identification

Product number -
Other names 2-Chloro-purine riboside

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:5466-11-5 SDS

5466-11-5Relevant academic research and scientific papers

Investigations into the origin of the molecular recognition of several adenosine deaminase inhibitors

Gillerman, Irina,Fischer, Bilha

experimental part, p. 107 - 121 (2011/03/19)

Inhibitors of adenosine deaminase (ADA, EC 3.5.4.4) are potential therapeutic agents for the treatment of various health disorders. Several highly potent inhibitors were previously identified, yet they exhibit unacceptable toxicities. We performed a SAR s

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