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72346-25-9

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72346-25-9 Usage

Classification

Synthetic nucleoside analogue.

Properties

Antiviral.

Mechanism of action

Inhibits the replication of a wide range of RNA and DNA viruses by interfering with their RNA-dependent RNA polymerase and DNA polymerase enzymes.

Primary uses

Treatment of hepatitis C, respiratory syncytial virus (RSV) infection, and certain viral hemorrhagic fevers.

Available forms

Oral capsules, tablets, and injections.

Side effects

Hemolytic anemia, teratogenicity, and birth defects.

Precaution

Use under the supervision of a healthcare professional.

Check Digit Verification of cas no

The CAS Registry Mumber 72346-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,4 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72346-25:
(7*7)+(6*2)+(5*3)+(4*4)+(3*6)+(2*2)+(1*5)=119
119 % 10 = 9
So 72346-25-9 is a valid CAS Registry Number.

72346-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-7H-purin-2-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:72346-25-9 SDS

72346-25-9Downstream Products

72346-25-9Relevant articles and documents

Autofluorescent fused-pyrimidine nucleosides: Synthesis and evaluation as permeants and inhibitors of human nucleoside transporters

Nowak, Ireneusz,Damaraju, Vijaya L.,Cass, Carol E.,Young, James D.,Robins, Morris J.

, p. 1395 - 1412 (2012/04/17)

Nucleosides with an aromatic five-membered ring heterocycle (N, O, or S) fused at C4-C5 of pyrimidin-2-one were prepared by ring closures with 5-(alkyn-1-yl)pyrimidin-2-one intermediates, heterocyclic atom replacements, and ring closure with a 5-aminocyti

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