Cas 153650-38-5,Phosphinous acid, diphenyl-, [(2S)-1-(diphenylphosphino)-5-oxo-2-pyrrolidinyl]methyl ester

153650-38-5

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Basic information

Product Name: Phosphinous acid, diphenyl-, [(2S)-1-(diphenylphosphino)-5-oxo-2-pyrrolidinyl]methyl ester
Synonyms:
CAS NO:153650-38-5
Molecular Formula: C29H27NO2P2
Molecular Weight: 483.486
EINECS: N/A
Product Categories: N/A
Mol File: 153650-38-5.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Phosphinous acid, diphenyl-, [(2S)-1-(diphenylphosphino)-5-oxo-2-pyrrolidinyl]methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Phosphinous acid, diphenyl-, [(2S)-1-(diphenylphosphino)-5-oxo-2-pyrrolidinyl]methyl ester(153650-38-5)
EPA Substance Registry System: Phosphinous acid, diphenyl-, [(2S)-1-(diphenylphosphino)-5-oxo-2-pyrrolidinyl]methyl ester(153650-38-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 153650-38-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 153650-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,6,5 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 153650-38:
(8*1)+(7*5)+(6*3)+(5*6)+(4*5)+(3*0)+(2*3)+(1*8)=125
125 % 10 = 5
So 153650-38-5 is a valid CAS Registry Number.

153650-38-5Upstream product

153650-38-5Downstream Products

153650-38-5Relevant academic research and scientific papers

New alkylarylamidophosphinephosphinites as chiral diphosphines for asymmetric hydrogenation of activated keto compounds

Roucoux,Agbossou,Mortreux,Petit

, p. 2279 - 2282 (1993)

Syntheses of new easily accessible chiral alkylarylamidophosphinephosphinite chelating ligands are described. Their rhodium complexes [Rh(L2*)Cl]2 are highly effective precursors for the catalytic asymmetric hydrogenation of functionalized ketones. Ketopantoyllactone and N-benzylphenyl glyoxamide are converted to the corresponding alcohols up to 96 and 79.6% ee respectively.

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