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50571-26-1

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50571-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50571-26-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,7 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50571-26:
(7*5)+(6*0)+(5*5)+(4*7)+(3*1)+(2*2)+(1*6)=101
101 % 10 = 1
So 50571-26-1 is a valid CAS Registry Number.

50571-26-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5'-O-dimethoxytritylthymidine 3'-H-phosphonate

1.2 Other means of identification

Product number -
Other names O5'-(4,4'-dimethoxy-trityl)-O3'-hydroxyphosphinoyl-thymidine

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:50571-26-1 SDS

50571-26-1Relevant articles and documents

First synthesis of carbocyclic oligothymidylates

Szemzo,Szecsi,Sagi,Otvos

, p. 1463 - 1466 (1990)

5'-O-(dimethoxytrityl)-(+)-carbocyclic thymidine 1 is converted into different 3'-substituted intermediates 2a-c following standard procedures. From these compounds stereochemically pure carbocyclic oligothymidylates 4 are obtained using solid phase synthetic methods.

Nucleoside H-phosphonates, XXII: Synthesis and properties of new nucleotide analogues - H-phosphonothiolate diesters

Hiresova, Renata,Stawinski, Jacek

, p. 2748 - 2752 (2008/03/14)

Condensation of nucleoside 3′-H-phosphonate monoesters with various thiols, promoted by condensing agents, provides a convenient access to a new class of H-phosphonate analogues, H-phosphonothiolate diesters. Chemical properties, relevant to possible appl

Use of ammonium aryl H-phosphonates in the preparation of nucleoside H-phosphonate building blocks

Ozola, Vita,Reese, Colin B.,Song, Quanlai

, p. 8621 - 8624 (2007/10/03)

Ammonium 4-methylphenyl H-phosphonate 4c was used in the conversion of 5'-0-(dimethoxy-trityl)-2'-deoxynucleoside derivatives 6 into the corresponding 3'-H-phosphonates 2, which were isolated in a high state of purity and in high yield.

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