Cas 480453-66-5,2-Diphenylphosphanyl-1-{(S)-2-[(diphenylphosphanyl)-methyl]-pyrrolidin-1-yl}-ethanone

480453-66-5

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Basic information

Product Name: 2-Diphenylphosphanyl-1-{(S)-2-[(diphenylphosphanyl)-methyl]-pyrrolidin-1-yl}-ethanone
Synonyms: 2-Diphenylphosphanyl-1-{(S)-2-[(diphenylphosphanyl)-methyl]-pyrrolidin-1-yl}-ethanone
CAS NO:480453-66-5
Molecular Formula:
Molecular Weight: 495.541
EINECS: N/A
Product Categories: N/A

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: 2-Diphenylphosphanyl-1-{(S)-2-[(diphenylphosphanyl)-methyl]-pyrrolidin-1-yl}-ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 2-Diphenylphosphanyl-1-{(S)-2-[(diphenylphosphanyl)-methyl]-pyrrolidin-1-yl}-ethanone(480453-66-5)
EPA Substance Registry System: 2-Diphenylphosphanyl-1-{(S)-2-[(diphenylphosphanyl)-methyl]-pyrrolidin-1-yl}-ethanone(480453-66-5)

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: 480453-66-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 480453-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,0,4,5 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 480453-66:
(8*4)+(7*8)+(6*0)+(5*4)+(4*5)+(3*3)+(2*6)+(1*6)=155
155 % 10 = 5
So 480453-66-5 is a valid CAS Registry Number.

480453-66-5Upstream product

3064-56-0 diphenylphosphinoacetic acid

480453-66-5Downstream Products

480453-66-5Relevant academic research and scientific papers

Examining the effect of hemilabile donor groups in non-C2 symmetrical terdentate ligands

Lam, Hubert,Cheng, Xiaohui,Steed, Jonathan W.,Aldous, David J.,Hii, King Kuok

, p. 5875 - 5877 (2002)

The type and position of donor atoms in proline-derived, non-C2 symmetric, terdentate ligands are found to have significant effects on the enantioselectivity of the palladium-catalysed allylic substitution reaction.

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