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34793-14-1

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34793-14-1 Usage

Type

Complex chemical compound

Purine Derivative

Contains a purine ring structure with an amino group at the 2-position and a thione group at the 6-position

Pentofuranosyl Group

Triply acetylated

Significance

Potential biological and pharmaceutical applications

Unique Properties

Modifications to the purine structure could lead to unique properties and activities valuable for drug development and research purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 34793-14-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,9 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34793-14:
(7*3)+(6*4)+(5*7)+(4*9)+(3*3)+(2*1)+(1*4)=131
131 % 10 = 1
So 34793-14-1 is a valid CAS Registry Number.

34793-14-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [3,4-diacetyloxy-5-(2-amino-6-sulfanylidene-3H-purin-9-yl)oxolan-2-yl]methyl acetate

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:34793-14-1 SDS

34793-14-1Downstream Products

34793-14-1Relevant articles and documents

A NEW METHOD FOR THE SYNTHESIS OF SOME 9-β-D-ARABINOFURANOSYLPURINES BY A COMBINATION OF CHEMICAL AND ENZYMATIC REACTIONS

Morisawa, Hirokazu,Utagawa, Takashi,Miyoshi, Takeshi,Yoshinaga, Fumihiro,Yamazaki, Akihiro,Mitsugi, Koji

, p. 479 - 482 (2007/10/02)

An enzymatic transarabinosylation between 2-chlorohypoxanthine and 1-β-D arabinofuranosyluracil gave 9-β-D-arabinofuranosyl-2-chlorohypoxanthine which was chemically converted to 9-β-D-arabinofuranosylguanine and its derivatives.

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