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Adenosine, N-benzoyl-5'-O-[(1,1-dimethylethyl)diphenylsilyl]-, 2',3'-diacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

201664-43-9

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201664-43-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201664-43-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,6,6 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 201664-43:
(8*2)+(7*0)+(6*1)+(5*6)+(4*6)+(3*4)+(2*4)+(1*3)=99
99 % 10 = 9
So 201664-43-9 is a valid CAS Registry Number.

201664-43-9SDS

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 2',3'-di-O-acetyl-N6-benzoyl-5'-O-[(tert-butyl)diphenylsilyl]adenosine

1.2 Other means of identification

Product number -
Other names Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-(6-benzoylamino-purin-9-yl)-2-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-3-yl ester

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:201664-43-9 SDS

201664-43-9Relevant academic research and scientific papers

Semisynthesis of 3′(2′)-O-(aminoacyl)-tRNA derivatives as ribosomal substrate

Cui, Zhiyong,Zhang, Biliang

, p. 297 - 310 (2008/02/08)

An efficient synthesis of (3′-terminally) 3′(2′)-O- aminoacylated pCpA derivatives is described, which could lead to the production of (aminoacyl)-tRNAs following T4 RNA ligase mediated ligation. The tetrahydrofuranyl (thf) group was used as a permanent p

Transprotection of N-benzoylated nucleobase derivatives by dialkylaminomethylene group

Endova, Magdalena,Masojidkova, Milena,Rosenberg, Ivan

, p. 2151 - 2164 (2007/10/03)

The use of (chloromethylene)dialkylammonium chloride in selective transprotection of N-benzoylated nucleobase derivatives is reported along with the evaluation of the stability of various protecting groups widely used in nucleoside and/or nucleotide chemi

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