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DIBENZYLPHOSPHOROCHLORIDITE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41662-50-4

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41662-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41662-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,6,6 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41662-50:
(7*4)+(6*1)+(5*6)+(4*6)+(3*2)+(2*5)+(1*0)=104
104 % 10 = 4
So 41662-50-4 is a valid CAS Registry Number.

41662-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name chloro-bis(phenylmethoxy)phosphane

1.2 Other means of identification

Product number -
Other names DIBENZYLPHOSPHOROCHLORIDITE

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:41662-50-4 SDS

41662-50-4Relevant academic research and scientific papers

Solventless synthesis of acyl phosphonamidates, precursors to masked bisphosphonates

Crossey, Kerri,Migaud, Marie E.

, p. 11088 - 11091 (2015/07/07)

A series of acyl phosphonamidates, the synthetic precursors to bisphosphonates, have been readily prepared from phosphoramidite type reagents and a range of acid chlorides. These reactions were performed using solventless conditions, where purification was easily achieved using column chromatography with yields ranging from 71-90%. Furthermore, we have demonstrated that these acyl phosphonamidates could be used for the preparation of unsymmetrical bisphosphonates, which do date are scarcely reported in the literature.

First Use of Benzyl Phosphites in the Michaelis-Arbuzov Reaction Synthesis of Mono-, Di-, and Triphosphate Analogs

Saady, Mourad,Lebeau, Luc,Mioskowski, Charles

, p. 670 - 678 (2007/10/02)

Benzyl phosphites were used in the Michaelis-Arbuzov reaction.Special experimental conditions allowed preparation of a set of phosphonate analogs of mono-, di-, and triphosphate.Furthermore, regioselective mono-deprotection mades these molecules useful building blocks for the synthesis of analogs of polyphosphorylated compounds of biological interest (e.g. nucleotides), after removal of all phosphonate benzyl ester groups under very mild conditions and high yields.

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