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72409-25-7

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72409-25-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72409-25-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,0 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72409-25:
(7*7)+(6*2)+(5*4)+(4*0)+(3*9)+(2*2)+(1*5)=117
117 % 10 = 7
So 72409-25-7 is a valid CAS Registry Number.

72409-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[9-[(2R,3R,4S,5R)-5-[[tert-butyl(dimethyl)silyl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]-6-oxo-3H-purin-2-yl]benzamide

1.2 Other means of identification

Product number -
Other names Guanosine,N-benzoyl-5'-O-[(1,1-dimethylethyl)dimethylsilyl]

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:72409-25-7 SDS

72409-25-7Downstream Products

72409-25-7Relevant articles and documents

Nucleotides, XVIII. Synthesis and Properties of (tert-Butyldimethylsilyl)guanosines, Guanosine-3'-Phosphotriesters and Guanosine-containing Oligonucleotides

Flockerzi, Dieter,Schlosser, Wilhelm,Pfleiderer, Wolfgang

, p. 2069 - 2085 (1983)

Silylation of N2-benzoyl- (1) and N2-isobutyrylguanosin (2) by tert-butyldimethylsilyl chloride led to the various mono-, di- and tri-O-tert-butyldimethylsilyl derivatives 3-15.The synthesis of 2'- (24-31) and 3'-phosphotriesters (16

NITRATE ION AS CATALYST FOR SELECTIVE SILYLATIONS OF NUCLEOSIDES

Hakimelahi, Gholam H.,Proba, Zbigniew A.,Ogilvie, Kelvin K.

, p. 4775 - 4778 (2007/10/02)

Nitrate ion has been found to have a remarkable effect on the selectivity of silylation of ribonucleosides using the t-butyldimethylsilyl group.

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