Cas 878293-72-2,[2,2'-bis(tert-butyl(phenyl)phosphino)diphenyl oxide]palladium dichloride

878293-72-2

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Basic information

Product Name: [2,2'-bis(tert-butyl(phenyl)phosphino)diphenyl oxide]palladium dichloride
Synonyms: [2,2'-bis(tert-butyl(phenyl)phosphino)diphenyl oxide]palladium dichloride
CAS NO:878293-72-2
Molecular Formula:
Molecular Weight: 675.911
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: [2,2'-bis(tert-butyl(phenyl)phosphino)diphenyl oxide]palladium dichloride(CAS DataBase Reference)
NIST Chemistry Reference: [2,2'-bis(tert-butyl(phenyl)phosphino)diphenyl oxide]palladium dichloride(878293-72-2)
EPA Substance Registry System: [2,2'-bis(tert-butyl(phenyl)phosphino)diphenyl oxide]palladium dichloride(878293-72-2)

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: 878293-72-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 878293-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,2,9 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 878293-72:
(8*8)+(7*7)+(6*8)+(5*2)+(4*9)+(3*3)+(2*7)+(1*2)=232
232 % 10 = 2
So 878293-72-2 is a valid CAS Registry Number.

878293-72-2Upstream product

878293-72-2Downstream Products

7440-05-3 palladium

878293-72-2Relevant academic research and scientific papers

Effect of steric and electronic properties of palladium complexes with bidentate diphosphine ligands on the basis of diphenyl oxide on arylation of amines

Veits,Mutsenek

, p. 207 - 211 (2005)

New complexes of palladium chloride with bidentate diphosphine ligands on the basis of 2,2′-bis(diorganylphosphino)diphenyl oxides were prepared by three methods, and their catalytic activity in arylation of amines was studied. 2005 Pleiades Publishing, Inc.

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