Cas 1429496-59-2,{(R)-(-)-4,12-bis[bis(3,4,5-trifluorophenyl)phosphino]-[2.2]-para-cyclophane}dipalladium(II) tetrachloride

1429496-59-2

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Basic information

Product Name: {(R)-(-)-4,12-bis[bis(3,4,5-trifluorophenyl)phosphino]-[2.2]-para-cyclophane}dipalladium(II) tetrachloride
Synonyms:
CAS NO:1429496-59-2
Molecular Formula:
Molecular Weight: 1147.2
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: {(R)-(-)-4,12-bis[bis(3,4,5-trifluorophenyl)phosphino]-[2.2]-para-cyclophane}dipalladium(II) tetrachloride(CAS DataBase Reference)
NIST Chemistry Reference: {(R)-(-)-4,12-bis[bis(3,4,5-trifluorophenyl)phosphino]-[2.2]-para-cyclophane}dipalladium(II) tetrachloride(1429496-59-2)
EPA Substance Registry System: {(R)-(-)-4,12-bis[bis(3,4,5-trifluorophenyl)phosphino]-[2.2]-para-cyclophane}dipalladium(II) tetrachloride(1429496-59-2)

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: 1429496-59-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1429496-59-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,9,4,9 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1429496-59:
(9*1)+(8*4)+(7*2)+(6*9)+(5*4)+(4*9)+(3*6)+(2*5)+(1*9)=202
202 % 10 = 2
So 1429496-59-2 is a valid CAS Registry Number.

1429496-59-2Upstream product

15617-18-2 bis(benzonitrile)palladium(II) dichloride

1429496-59-2Downstream Products

1429496-59-2Relevant academic research and scientific papers

Simultaneous control of regioselectivity and enantioselectivity in the hydroxycarbonylation and methoxycarbonylation of vinyl arenes

Konrad, Tina M.,Durrani, Jamie T.,Cobley, Christopher J.,Clarke, Matthew L.

, p. 3306 - 3308 (2013)

Using a family of novel mononuclear and dinuclear palladium complexes of phanephos ligands, the simultaneous control of regioselectivity and enantioselectivity in the hydroxycarbonylation and alkoxycarbonylation of styrene derivatives has been realised for the first time. The Royal Society of Chemistry 2013.

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