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Phosphinic acid, ethenylphenyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119073-93-7

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119073-93-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119073-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,0,7 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 119073-93:
(8*1)+(7*1)+(6*9)+(5*0)+(4*7)+(3*3)+(2*9)+(1*3)=127
127 % 10 = 7
So 119073-93-7 is a valid CAS Registry Number.

119073-93-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [ethenyl(methoxy)phosphoryl]benzene

1.2 Other means of identification

Product number -
Other names Phenyl-vinyl-phosphinsaeure-methylester

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:119073-93-7 SDS

119073-93-7Relevant academic research and scientific papers

Stereoselective catalytic synthesis of P-stereogenic oxides via hydrogenative kinetic resolution

Fernández-Pérez, Héctor,Vidal-Ferran, Anton

supporting information, p. 7019 - 7023 (2019/09/30)

A highly stereoselective catalytic method for the preparation of structurally diverse P-stereogenic oxides has been developed. The approach relies on the ability of rhodium complexes derived from an enantiopure P-OP ligand to kinetically resolve racemic α,β-unsaturated phosphane oxides by hydrogenation of the C= C motif and formation of highly enantioenriched (or even enantiopure) P-stereogenic oxides. The practicality of the methodology has been demonstrated by the preparation of potentially functional P-chiral molecules for catalytic enantioselective synthesis.

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