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77180-90-6

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77180-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77180-90-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,8 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77180-90:
(7*7)+(6*7)+(5*1)+(4*8)+(3*0)+(2*9)+(1*0)=146
146 % 10 = 6
So 77180-90-6 is a valid CAS Registry Number.

77180-90-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-FLUORO-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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:77180-90-6 SDS

77180-90-6Relevant 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.

Preparation, antibacterial effects and enzymatic degradation of 5-fluorouracil nucleosides

Schwarz,Cech,Holy,Skoda

, p. 3217 - 3230 (2007/10/02)

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