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117309-93-0

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117309-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117309-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,3,0 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 117309-93:
(8*1)+(7*1)+(6*7)+(5*3)+(4*0)+(3*9)+(2*9)+(1*3)=120
120 % 10 = 0
So 117309-93-0 is a valid CAS Registry Number.

117309-93-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-1-[(6R,7R)-2,7-dihydroxy-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-5-hexylpyrimidin-2-one

1.2 Other means of identification

Product number -
Other names 5-n-Hexylcytidine 3',5'-cyclic monophosphate

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:117309-93-0 SDS

117309-93-0Downstream Products

117309-93-0Relevant articles and documents

Synthesis and Cytostatic and Antiviral Activities of 1-β-D-Ribofuranosyl-5-alkylcytosine (5-Alkylcytidine) Cyclic 3',5'-Monophosphates

Beres, Jozsef,Bentrude, Wesley G.,Oetvoes, Laszlo,Balzarini, Jan,Clercq, Erik De

, p. 224 - 228 (2007/10/02)

A series of 5-alkylcytidines and their 5'-monophosphates and cyclic 3',5'-monophosphates have been synthesized and evaluated for antiviral and antitumor activity.The 5-alkyl cyclic nucleotides were not cytostatic (ID 50 > 200 μg/mL) against leukemia L1210 cells and a deoxycytidine kinase-deficient subline thereof.Certain of the corresponding nucleosides and their 5'-monophosphates did show activity within the range of 35-162 μg/mL, as did the unsubstituted cytidine cyclic 3',5'-monophosphate.No antiviral activity was found for any of the compounds at 400 μg/mL.A drug design rationale for utilization of 5-alkylcytidines based on their potential conversion to biologically active 5-alkyl-2'-deoxyuridines is not supported by these experimental findings.

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