Cas 1449602-62-3,bis(4-bromophenyl){3-[1-(4-bromophenyl)-2,2-diphenylvinyl]naphthalen-2-yl}phosphine

1449602-62-3

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Basic information

Product Name: bis(4-bromophenyl){3-[1-(4-bromophenyl)-2,2-diphenylvinyl]naphthalen-2-yl}phosphine
Synonyms: bis(4-bromophenyl){3-[1-(4-bromophenyl)-2,2-diphenylvinyl]naphthalen-2-yl}phosphine
CAS NO:1449602-62-3
Molecular Formula:
Molecular Weight: 803.37
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: bis(4-bromophenyl){3-[1-(4-bromophenyl)-2,2-diphenylvinyl]naphthalen-2-yl}phosphine(CAS DataBase Reference)
NIST Chemistry Reference: bis(4-bromophenyl){3-[1-(4-bromophenyl)-2,2-diphenylvinyl]naphthalen-2-yl}phosphine(1449602-62-3)
EPA Substance Registry System: bis(4-bromophenyl){3-[1-(4-bromophenyl)-2,2-diphenylvinyl]naphthalen-2-yl}phosphine(1449602-62-3)

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: 1449602-62-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1449602-62-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,6,0 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1449602-62:
(9*1)+(8*4)+(7*4)+(6*9)+(5*6)+(4*0)+(3*2)+(2*6)+(1*2)=173
173 % 10 = 3
So 1449602-62-3 is a valid CAS Registry Number.

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1449602-62-3Relevant academic research and scientific papers

Nickel-catalyzed manipulation of tertiary phosphines via highly selective C-P bond cleavage

Cao, Jian,Huang, Xian,Wu, Luling

supporting information, p. 7747 - 7749 (2013/09/02)

A catalytic cycle involving oxidative addition of nickel(0) with a carbon-carbon single bond in the three-membered ring of diarylmethylenecyclopropa[b]naphthalenes, highly selective cleavage of the C-P bond, and migration of the aryl group of phosphine consequently provides a new type of bulky phosphine in excellent yields.

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