Cas 326607-13-0,(2-C6H4(Et))2PN(Me)P(2-C6H4(Et))2

326607-13-0

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Basic information

Product Name: (2-C₆H₄(Et))2PN(Me)P(2-C₆H₄(Et))2
Synonyms: (2-C₆H₄(Et))2PN(Me)P(2-C₆H₄(Et))2
CAS NO:326607-13-0
Molecular Formula:
Molecular Weight: 511.627
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-C₆H₄(Et))2PN(Me)P(2-C₆H₄(Et))2(CAS DataBase Reference)
NIST Chemistry Reference: (2-C₆H₄(Et))2PN(Me)P(2-C₆H₄(Et))2(326607-13-0)
EPA Substance Registry System: (2-C₆H₄(Et))2PN(Me)P(2-C₆H₄(Et))2(326607-13-0)

Safety Data

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Safety Statements: N/A
WGK Germany:
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HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 326607-13-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 326607-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,6,6,0 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 326607-13:
(8*3)+(7*2)+(6*6)+(5*6)+(4*0)+(3*7)+(2*1)+(1*3)=130
130 % 10 = 0
So 326607-13-0 is a valid CAS Registry Number.

326607-13-0Upstream product

326607-13-0Downstream Products

1018433-77-6 [Cr(CO)4((2-C₆H₄(Et))2PN(Me)P(2-C₆H₄(Et))2)]

326607-13-0Relevant academic research and scientific papers

POLYMERISATION PROCESS CATALYSED BY A BIDENTATE BISPHOSPHINE-GROUP VIII METAL COMPLEX

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Page/Page column 9-10, (2010/11/27)

A process for the polymerization and copolymerization of olefins is disclosed, comprising contacting the monomeric olefin under polymerization conditions with a polymerization catalyst or catalyst system which comprises (a) a source of a Group VIII metal; (b) a bidentate phosphine ligand having the formula (R1)(R1)P-X-P(R1)(R1), where each R1 is independently selected from a phenyl group or a substitued phenyl group with the proviso that at least one of the R1 groups is a phenyl group having at least one ortho substituent, and X is a bridging group of the structure -[N]x-[P]y-[N]- where x and y are independently 0 or 1, or -C(R4)2- where R4 may be the same or different and is hydrogen or a monovavlent hydrocarbyl, substituted hydrocarbyl or hetero-hydrocarbyl group; and optionally (c) a promoter.

Highly selective chromium-based ethylene trimerisation catalysts with bulky diphosphinoamine ligands

Blann, Kevin,Bollmann, Annette,Dixon, John T.,Hess, Fiona M.,Killian, Esna,Maumela, Hulisani,Morgan, David H.,Neveling, Arno,Otto, Stephanus,Overett, Matthew J.

, p. 620 - 621 (2007/10/03)

In situ prepared chromium catalysts containing bulky diphosphinoamine (PNP) ligands, upon activation with MAO, are extremely efficient catalysts for the trimerisation of ethylene to 1-hexene. The Royal Society of Chemistry 2005.

Steric activation of chelate catalysts: Efficient polyketone catalysts based on four-membered palladium(II) diphosphine chelates

Dossett,Gillon,Orpen,Fleming,Pringle,Wass,Jones

, p. 699 - 700 (2007/10/03)

Palladium(II) complexes of ligands of the type Ar2PCH2-PAr2 and Ar2PN(Me)PAr2 (Ar = ortho-substituted phenyl group) are very efficient catalysts for copolymerisation of CO and C2H4/su

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