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O5'-(4,4'-dimethoxy-trityl)-2'-deoxy-[3']cytidylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

214535-14-5

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214535-14-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214535-14-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,5,3 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 214535-14:
(8*2)+(7*1)+(6*4)+(5*5)+(4*3)+(3*5)+(2*1)+(1*4)=105
105 % 10 = 5
So 214535-14-5 is a valid CAS Registry Number.

214535-14-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name O5'-(4,4'-dimethoxy-trityl)-2'-deoxy-[3']cytidylic acid

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:214535-14-5 SDS

214535-14-5Downstream Products

214535-14-5Relevant academic research and scientific papers

A facile method for the oxidation of nucleoside H-phosphonates to phosphates with bis(trimethylsilyl) peroxide

Kato, Toru,Hayakawa, Yoshihiro

, p. 1796 - 1798 (2007/10/03)

We have developed a convenient method for achieving the oxidation of nucleoside H-phosphonic acid monoesters and diesters with bis(trimethylsilyl) peroxide and N,O-bis(trimethylsilyl)acetamide in the presence of trimethylsilyl triflate as a catalyst.

Electrochemical removal of allylic protecting groups in nucleotide synthesis

Hayakawa, Yoshihiro,Kawai, Rie,Wakabayashi, Shigeharu,Uchiyama, Mamoru,Noyori, Ryoji

, p. 441 - 449 (2007/10/03)

Electrochemical, palladium(0)-mediated removal of allylic protecting groups of nucleosides and nucleotides is described. This method required no chromatographic treatment for isolation of the products.

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