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7392-74-7

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  • Factory Price API 99% 2,3,5-Tri-O-benzoyl-2-C-methyl-D-ribonic acid-1,4-lactone 7392-74-7 GMP Manufacturer

    Cas No: 7392-74-7

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7392-74-7 Usage

Chemical Properties

White Powder

Uses

2,3,5-Tri-O-benzoyl-2-C-methyl-D-ribonic-1,4-lactone (cas# 7392-74-7) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 7392-74-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7392-74:
(6*7)+(5*3)+(4*9)+(3*2)+(2*7)+(1*4)=117
117 % 10 = 7
So 7392-74-7 is a valid CAS Registry Number.

7392-74-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3R,4R)-3,4-dibenzoyloxy-4-methyl-5-oxooxolan-2-yl]methyl benzoate

1.2 Other means of identification

Product number -
Other names 2,3,4,6-TETRA-O-ACETYL-1-O-TRICHLOROACETIMIDOYL-

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:7392-74-7 SDS

7392-74-7Relevant articles and documents

SUBSTITUTED NUCLEOSIDES, NUCLEOTIDES AND ANALOGS THEREOF

-

Paragraph 0304, (2018/03/06)

Disclosed herein are nucleotide analogs, methods of synthesizing nucleotide analogs and methods of treating diseases and/or conditions such as a Picornaviridae and/or Flaviviridae viral infections with one or more nucleotide analogs.

Synthesis and Evaluation of 2,6-Modified Purine 2′-C-Methyl Ribonucleosides as Inhibitors of HCV Replication

Zhou, Longhu,Zhang, Hongwang,Tao, Sijia,Ehteshami, Maryam,Cho, Jong Hyun,McBrayer, Tamara R.,Tharnish, Philip,Whitaker, Tony,Amblard, Franck,Coats, Steven J.,Schinazi, Raymond F.

supporting information, p. 17 - 22 (2016/02/03)

A variety of 2,6-modified purine 2′-C-methylribonucleosides and their phosphoramidate prodrugs were synthesized and evaluated for inhibition of HCV RNA replication in Huh-7 cells and for cytotoxicity in various cell lines. Cellular pharmacology and HCV polymerase incorporation studies on the most potent and selective compound are reported.

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