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131173-04-1

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131173-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131173-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,1,7 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 131173-04:
(8*1)+(7*3)+(6*1)+(5*1)+(4*7)+(3*3)+(2*0)+(1*4)=81
81 % 10 = 1
So 131173-04-1 is a valid CAS Registry Number.

131173-04-1 Well-known Company Product Price

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  • Aldrich

  • (738166)  N,N-Diisopropyl-P,P-diphenylphosphinamide  97%

  • 131173-04-1

  • 738166-1G

  • 267.93CNY

  • Detail

131173-04-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-diphenylphosphoryl-N-propan-2-ylpropan-2-amine

1.2 Other means of identification

Product number -
Other names N,N-Diisopropyl-P,P-diphenylphosphinamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:131173-04-1 SDS

131173-04-1Relevant articles and documents

New: O-substituted diphenylphosphinic amide ligands: Synthesis, characterization and complexation with Zn2+, Cu2+ and Y3+

Rodrigues Furtado Medeiros, Ant?nia Carlene,Gouvea, Marcos Martins,Felipe, Thaian Vieira,Marques, Flávia Ferreira De Carvalho,Bernardino, Alice Maria Rolim,López Ortiz, Fernando,De Souza, Marcos Costa

, p. 13881 - 13890 (2019/09/18)

Phosphinic amide derivatives have drawn significant attention in coordination chemistry and have been incorporated into the design and synthesis of new ligands. In this work, the combination of the diphenylphosphinic amide group with quinoline, pyridine a

Ethylene Polymerization and Copolymerization with Polar Monomers by Cationic Phosphine Phosphonic Amide Palladium Complexes

Sui, Xuelin,Dai, Shengyu,Chen, Changle

, p. 5932 - 5937 (2015/10/12)

The synthesis, characterization, and olefin (co)polymerization studies of a series of palladium complexes bearing phosphine phosphonic amide ligands were investigated. In this ligand framework, substituents on three positions could be modulated independently, which distinguishes this class of ligand and provides a great deal of flexibilities and opportunities to tune the catalytic properties. The palladium complex with an o-MeO-Ph substituent on phosphine is one of the most active palladium catalysts in ethylene polymerization, with 1 order of magnitude higher activity than the corresponding classic phosphine-sulfonate palladium complex. Meanwhile, the polyethylene generated by this new palladium complex showed ca. 6 times higher molecular weight in comparison to that by the classic phosphine-sulfonate palladium complex. In ethylene/methyl acrylate copolymerization, the new palladium complex showed lower activity, generating copolymer with similar methyl acrylate incorporation and much higher molecular weight. The new palladium complex was also able to copolymerize ethylene with other polar monomers, including butyl vinyl ether and allyl acetate, making it one of the very few catalyst systems that can copolymerize ethylene with multiple industrially relevant polar monomers.

Directed ortho metallation chemistry and phosphine synthesis: New ligands for the suzuki-miyaura reaction

Williams, D. Bradley G.,Evans, Stephen J.,De Bod, Henriette,Mokhadinyana, Molise S.,Hughes, Tanya

experimental part, p. 3106 - 3112 (2009/12/28)

We describe the use of the phosphinic amide moiety as an effective directed ortho metallation group for the incorporation of various phosphino groups onto a benzene ring to generate phosphine ligands. These ligands were used to generate active palladium c

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