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725257-84-1

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  • 5-FLUORO-4-THIO-1-(2'', 3'', 5''-TRI-O-BENZOYL-β-L-RIBOFURANOSYL)URACIL

    Cas No: 725257-84-1

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725257-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 725257-84-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,5,2,5 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 725257-84:
(8*7)+(7*2)+(6*5)+(5*2)+(4*5)+(3*7)+(2*8)+(1*4)=171
171 % 10 = 1
So 725257-84-1 is a valid CAS Registry Number.

725257-84-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-FLUORO-4-THIO-1-(2'', 3'', 5''-TRI-O-BENZOYL-β-L-RIBOFURANOSYL)URACIL

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

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More Details:725257-84-1 SDS

725257-84-1Downstream Products

725257-84-1Relevant articles and documents

Stereospecific synthesis and biological evaluations of β-L-pentofuranonucleoside derivatives of 5-fluorouracil and 5-fluorocytosine

Griffon, Jean-Francois,Mathe, Christophe,Faraj, Abdesslem,Aubertin, Anne-Marie,De Clercq, Erik,Balzarini, Jan,Sommadossi, Jean-Pierre,Gosselin, Gilles

, p. 447 - 460 (2007/10/03)

In the search for new chemotherapeutic agents, we have focused our work on the synthesis and the study of several unnatural β-L-nucleoside analogues. In this paper, we report on the synthesis of β-L-pentofuranonucleosides (and their 2′-deoxy derivatives) of 5-fluorouracil and their inhibitory effects on the proliferation of several murine and human tumor cells. The corresponding 5-fluorocytosine derivatives were also synthesized and their anti-HIV and anti-HBV activities have been evaluated.

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