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124355-34-6

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124355-34-6 Usage

Chemical class

Nucleoside analog

Antiviral properties

Yes

Target viruses

Herpes viruses

Mechanism of action

Interferes with viral DNA replication

Commonly used form

Antiviral medications

Effective in treating

Genital herpes, shingles, and chickenpox

Chemical structure

Pyrimidine-2,4-dione ring and a triazole group

Potential side effects

Nausea, vomiting, and headache

Usage guidance

Should be used with caution under the guidance of a healthcare professional

Check Digit Verification of cas no

The CAS Registry Mumber 124355-34-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,5 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 124355-34:
(8*1)+(7*2)+(6*4)+(5*3)+(4*5)+(3*5)+(2*3)+(1*4)=106
106 % 10 = 6
So 124355-34-6 is a valid CAS Registry Number.

124355-34-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2R,3S,4S,5S)-3-hydroxy-5-(hydroxymethyl)-4-(1,2,4-triazol-1-yl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione

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:124355-34-6 SDS

124355-34-6Downstream Products

124355-34-6Relevant articles and documents

Synthesis and Antiviral Activity of 3'-Heterocyclic Substituted 3'-Deoxythymidines

Wigerinck, Piet,Aerschot, Arthur Van,Janssen, Gerard,Claes, Paul,Balzarini, Jan,et al.

, p. 868 - 873 (2007/10/02)

Various 3'-deoxythymidine analogues with an heterocyclic five-membered ring in the 3'-erythro position have been synthesized.The pyrrol-1-yl (3) and the 1,2,4-triazol-4-yl (5) compounds were synthesized from 1-(3-amino-2,3-dideoxy-β-D-erythro-pentofuranosyl)thymine.The pyrazol-1-yl (16a), imidazol-1-yl (16b), and 1,2,4-triazol-1-yl (16c) derivatives were obtained by epoxide opening of the corresponding 1-(2,3-anhydro-β-D-lyxofuranosyl)thymines followed by 2'-deoxygenation.Only the 3'-pyrrol-1-yl derivative showed marginal antiviral activity against human immunodeficiency virus.

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