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Bis(isopropyl-amino)-phenylphosphine, also known as diisopropyl(phenyl)phosphine, is an organophosphorus compound with the chemical formula C12H20NP. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 221.27 g/mol. bis(isopropyl-amino)-phenylphosphine is primarily used as a ligand in homogeneous catalysis, particularly in the field of transition metal catalysis. It plays a crucial role in various chemical reactions, such as hydroformylation, hydrogenation, and olefin polymerization, by stabilizing and activating metal catalysts. Bis(isopropyl-amino)-phenylphosphine is also known for its ability to form stable complexes with metals, which can enhance the selectivity and activity of catalytic processes. Due to its importance in catalysis, it is a subject of ongoing research in the field of organometallic chemistry and industrial chemistry.

716-85-8

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716-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 716-85-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 716-85:
(5*7)+(4*1)+(3*6)+(2*8)+(1*5)=78
78 % 10 = 8
So 716-85-8 is a valid CAS Registry Number.

716-85-8Relevant academic research and scientific papers

Catalyst composition and process for di-, tri- and/or tetramerization of ethylene

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Page/Page column 7, (2014/02/16)

The present invention relates to a catalyst composition and a process for di-, tri- and/or tetramerization of ethylene, wherein the catalyst composition comprises a chromium compound, a ligand of the general structure (A) R1R2P—N(Rs

METHOD FOR PURIFYING A CRUDE PNPNH COMPOUND

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Paragraph 0044, (2014/08/19)

The present invention relates to a method for purifying a crude PNPNH compound by metalation and re-protonation.

METHOD FOR PURIFYING A CRUDE PNPNH COMPOUND

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Paragraph 0046, (2014/08/19)

A method for purifying a crude PNPNH compound of the general structure [in-line-formulae]R1R2P—N(R3)—P(R4)—N(R5)—H[/in-line-formulae] wherein R1, R2, R3, R4 /sub

METALATED LIGAND, CATALYST COMPOSITION, AND USE THEREOF IN THE OLIGOMERIZATION OF ETHYLENE

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Paragraph 0064, (2014/08/19)

A process for oligomerization of ethylene, comprising subjecting a catalyst composition to a gas phase of ethylene and conducting an oligomerization, wherein the catalyst composition comprises (a) a chromium compound, (b) a metalated ligand, and (c) an ac

Synthesis of differently substituted N- and P-aminodiphosphinoamine PNPN-H ligands

Gongoll, Marc,Mueller, Bernd H.,Peitz, Stephan,Aluri, Bhaskar R.,Peulecke, Normen,Spannenberg, Anke,Rosenthal, Uwe,Al-Hazmi, Mohammed H.,Woehl, Anina,Mueller, Wolfgang

, p. 1845 - 1854 (2013/11/06)

On the basis of the known aminodiphosphinoamine ligand Ph 2PN(i-Pr)P(Ph) N(i-Pr)-H (3a), differently substituted aminodiphosphinoamine PNPN-H ligands (3) were prepared. By using different synthetic methods, the N-substituted ligands Ph2/s

Synthesis and reactions of the homoleptic chromium(II) bis-amide [Ph 2PN(iPr)P(Ph)N(iPr)-]2Cr with relevance to a selective catalytic ethene trimerization system to 1-hexene

Mueller, Bernd H.,Peulecke, Normen,Spannenberg, Anke,Rosenthal, Uwe,Al-Hazmi, Mohammed H.,Schmidt, Roland,Woehl, Anina,Mueller, Wolfgang

scheme or table, p. 3695 - 3699 (2012/06/30)

New organometallic compounds were obtained on the basis of the aminodiphosphinoamine ligand Ph2PN(iPr)P(Ph)N( iPr)-H (1), which is relevant for the selective ethene trimerization system consisting of ligand 1, CrCl3/

N, N′-bis(diphenylphosphino)diaminophenylphosphine ligands for chromium-catalyzed selective ethylene oligomerization reactions

Dulai, Arminderjit,McMullin, Claire L.,Tenza, Kenny,Wass, Duncan F.

experimental part, p. 935 - 941 (2011/05/03)

Reaction of 1 or 2 equiv of Ph2PCl with PhP(N(H)R)2 (R = n-propyl) yields Ph2PN(R)P(Ph)N(R)H (1) or Ph 2PN(R)P(Ph)N(R)PPh2 (2), respectively. In contrast, reaction of 1 or 2 equiv of Ph2PCl with PhP(N(H)R)2 (R = isopropyl) yields exclusively Ph2PN(R)P(Ph)N(R)H (3), even under more forcing conditions. Low-temperature NMR spectroscopy and a conformational analysis of Ph2PN(iPr)P(Ph)N(iPr)H (3) reveal the lowest energy conformer to have a close N-H???P interaction of 2.95 A, which we speculate may hinder further reactivity of this molecule. Reaction of 3 with [Cr(CO)6] yields [Cr(3)(CO)4] (5), which has been structurally characterized. Coordination of ligand 3 facilitates its conversion to Ph2PN(iPr)P(Ph)N(iPr)PPh2 (4) while bound to chromium, yielding the complex [Cr(4)(CO)4] (6), which has also been structurally characterized. Ligands 1 and 2, when reacted in situ with [Cr(acac)3] (acac = acetylacetonate) and modified methylalumoxane, and complexes 5 and 6, when activated with Ag[Al(OC4F 9)4] and triethylaluminum, are moderately active and selective catalysts for the selective oligomerization of ethene to 1-hexene and 1-octene.

(N-lithioamino)diorganophosphanes and bis(N- lithioamino)organophosphanes: Synthesis and structures

Eichhorn, Bettina,Noeth, Heinrich,Seifert, Thomas

, p. 2355 - 2368 (2007/10/03)

Butyllithium (nBuLi) deprotonates Ph2P-NHtBu in ether to give (Ph2P- NLitBu)2 · OEt2. There is no Li ··· P interaction in this molecule. Three compounds of the type R'P(NLiR)2 have been obtained by li

LES PHOSPHORANES MONOCYCLIQUES A LIAISON PH DANS LES REACTIONS DE REDISTRIBUTION DE LIGANDS DES COMPOSES DU PHOSPHORE TRICOORDONNE

Tangour, B.,Malavaud, C.,Boisdon, M. T.,Barrans, J.

, p. 189 - 196 (2007/10/02)

The oxidative addition of alcohols and amines with 2-alkyl, 2-aryl, 1,3,2-dioxa, oxaza or diazaphospholanes, leads to a ring opening reaction and ligands exchange around the phosphorus atom by alcoholysis or aminolysis of P-O or P-N bonds.In nearly all cases, monocyclic phosphoranes with P-H bond have been detected in an intermediate step during the exchange of one tricoordinate form to another one.At last we have discussed the phorpholanyl ring stability. - Key words: 1,3,2-Dioxaphospholanes; 1,3,2-oxaza-phospholanes; 1,3,2-diazaphospholanes; Monocyclic phosphoranes with P-M bonds; phosphoranyl ring stability.

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