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1201795-29-0

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1201795-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1201795-29-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,7,9 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1201795-29:
(9*1)+(8*2)+(7*0)+(6*1)+(5*7)+(4*9)+(3*5)+(2*2)+(1*9)=130
130 % 10 = 0
So 1201795-29-0 is a valid CAS Registry Number.

1201795-29-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl tosyloxymethanephosphonate

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:1201795-29-0 SDS

1201795-29-0Relevant articles and documents

Methyl 4-toluenesulfonyloxymethylphosphonate, a new and versatile reagent for the convenient synthesis of phosphonate-containing compounds

Kó?iová, Ivana,To?ík, Zdeněk,Budě?ínsky, Milo?,?imák, Ond?ej,Liboska, Radek,Rejman, Dominik,Pa?es, Ond?ej,Rosenberg, Ivan

supporting information; experimental part, p. 6745 - 6747 (2010/05/03)

A straightforward procedure leading to the new phosphonylating reagent, methyl 4-toluenesulfonyloxymethylphosphonate, requiring no chromatographic purification is described. This stable reagent works with the same efficiency as dimethyl and other dialkyl esters for the introduction of an O-phosphonomethyl moiety while, in contrast to dimethyl ester, it does not cause any unwanted methylation of sensitive functionalities. Its utility for the alkylation of protected nucleosides in high yield is exemplified.

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