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Phosphinic acid, (aminophenylmethyl)phenyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

121197-47-5

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121197-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121197-47-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,1,9 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 121197-47:
(8*1)+(7*2)+(6*1)+(5*1)+(4*9)+(3*7)+(2*4)+(1*7)=105
105 % 10 = 5
So 121197-47-5 is a valid CAS Registry Number.

121197-47-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl α-aminobenzyl(phenyl)phosphinate

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:121197-47-5 SDS

121197-47-5Relevant academic research and scientific papers

A recyclable chiral auxiliary for the asymmetric syntheses of α-aminonitriles and α-aminophosphinic derivatives

Rossi, Jean-Christophe,Marull, Marc,Larcher, Nicolas,Taillades, Jacques,Pascal, Robert,van der Lee, Arie,Gerbier, Phillipe

, p. 876 - 883 (2008/09/21)

Optically active α-aminonitriles and α-aminophosphinic derivatives have been prepared in high yield and high ee using an easy route by extending our previously developed method involving the following sequence: (i) stereoselective Strecker condensation of

Interesting by-products in the synthesis of chiral α- aminophosphinates from enantiopure sulfinimines

Szabó, Andrea,Jászay, Zsuzsa M.,T?ke, László,Petneházy, Imre

, p. 1991 - 1994 (2007/10/03)

A new reaction of enantiopure sulfinimines and ethyl phenylphosphinate is given. Several unexpected products were isolated and identified, their mechanism of formation is proposed.

A CONVENIENT SYNTHESIS OF O-ETHYL-1-AMINOALKYLPHOSPHINATES

Gajda, Tadeusz

, p. 59 - 64 (2007/10/02)

1-Aminoalkylphosphinates 4 have been obtained in good yields in a one-step transformation by the Mitsunobu reaction of 1-hydroxyalkylphosphinates 1 with hydrazoic acid, and subsequent treatment of the intermediate azides 2, with triphenylphosphine, follow

Studies on Organophosphorus Compounds XXVIII. An Improved Synthetic Route to 1-Amino-Substituted Benzyl Phosphonic and -Phosphinic Acids

Yuan, Chengye,Qi, Youmao

, p. 472 - 474 (2007/10/02)

An improved method for the synthesis of 1-aminosubstituted benzyl phosphonic and -phosphinic acids under mild conditions is described.It consists of the reaction of diphenoxy chlorophosphine (1) or dichlorophenylphosphine (6) with substituted benzaldehyde

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