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Phosphinous acid, diphenyl-, [1-(diphenylphosphino)-2-pyrrolidinyl]methyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83728-79-4

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83728-79-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83728-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,2 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83728-79:
(7*8)+(6*3)+(5*7)+(4*2)+(3*8)+(2*7)+(1*9)=164
164 % 10 = 4
So 83728-79-4 is a valid CAS Registry Number.

83728-79-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-(N-diphenylphosphino)(2-diphenylphosphinoxymethyl)pyrrolidine

1.2 Other means of identification

Product number -
Other names (S)-N-(diphenylphosphino)-2-diphenylphosphinoxymethylpyrrolidine, (S)-prolophos

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:83728-79-4 SDS

83728-79-4Downstream Products

83728-79-4Relevant academic research and scientific papers

Highly selective synthesis of 4-vinylcyclohexene by cyclodimerization of butadiene catalysed by aminophosphinephosphinite and bis(aminophosphine) chiral ligands nickel complexes

Suisse, Isabelle,Bricout, Herve,Mortreux, Andre

, p. 413 - 416 (2007/10/02)

The highest chemoselective synthesis of 4-vinylcyclohexene ever observed by butadiene cyclodimerization on nickel complexes has been obtained with aminophosphinephosphinite and bis(aminophosphine) chiral ligands (selectivity up to 99%).

ASYMMETRIC HYDROGENATION CATALYZED BY AMINOPHOSPHINE-PHOSPHINITERHODIUM COMPLEXES DERIVED FROM NATURAL AMINOALCOHOLS AND X-RAY CRYSTAL STRUCTURE OF (1,5-CYCLOOCTADIENE)-(S)-N-(DIPHENYLPHOSPHINO)-2-DIPHENYLPHOSPHINOXYMETHYLPYRROLIDINERHODIUM(I) PERCHLORATE

Cesarotti, E.,Chiesa, A.,Ciani, G.,Sironi, A.

, p. 79 - 92 (2007/10/02)

From the cheap and readily available amino alcohols (S)-pyrrolidinemethanol ((S)-prolinol), and (S)-α-N-ethyl-aminobutanol, we have obtained two new aminophosphine-phosphinite ligands: (S)-N-(diphenylphosphino)-2-diphenylphosphinooxymethylpyrrolidine ((S)-Prolophos) and (S)-1-diphenylphosphinoxy-2-N-ethyl-N-diphenylphosphinoaminobutane ((S)-Butaphos).The rhodium(I) complexes of these phosphines act as efficient homogeneous hydrogenation catalysts at ambient temperature and pressures for dehydro N-acetyl amono acids, dehydro N-benzoyl amino acids and itaconic acid.An X-ray diffraction study of the complex *THF has been shown that the crystals belong to the monoclinic space group P21 with a 10.680(2), b 10.448(2), c 18.207(3) Angstroem and β 104.97(1)o.Refinements based on 2105 significant counter reflections led to a final R value of 0.060.The cation is in a distorted square planar geometry, the rhodium atom being bound to the two phosphorus atoms and to the two double bonds of the diene molecule.

ASYMMETRIC HYDROGENATION BY CHIRAL AMINOPHOSPHINE-PHOSPHINITE RHODIUM COMPLEXES

Cesarotti, E.,Chiesa, A.,D'Alfonso, G.

, p. 2995 - 2996 (2007/10/02)

The ligands (S)-N-(diphenylphosphino)-2-diphenylphosphinomethylpyrrolidine, (S)-prolophos, and (S)-1-diphenylphosphinoxy-2-N-ethyl-N-diphenylphosphinoaminobutane,(S)-butaphos, have been prepared.The Rh(I) complexes of these phosphines act as an efficient homogenous hydrogenation catalysts at ambient temperature and pressure for α-N-acetaminoacrylic acid and itaconic acid.

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