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Tris-(4-pentyl-phenyl)-phosphane, also known as tri(4-pentylphenyl)phosphine, is an organophosphorus compound with the chemical formula C27H39P. It is a colorless, crystalline solid that is soluble in organic solvents. Tris-(4-pentyl-phenyl)-phosphane is characterized by its three 4-pentylphenyl groups attached to a central phosphorus atom, which gives it unique chemical properties. It is primarily used as a ligand in homogeneous catalysis, particularly in the field of transition metal chemistry, where it can help stabilize and modulate the activity of metal catalysts. The steric bulk of the pentyl groups can influence the selectivity and reactivity of the catalysts, making it a valuable tool in synthetic chemistry for the development of new reactions and processes.

76287-44-0

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76287-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76287-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,8 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76287-44:
(7*7)+(6*6)+(5*2)+(4*8)+(3*7)+(2*4)+(1*4)=160
160 % 10 = 0
So 76287-44-0 is a valid CAS Registry Number.

76287-44-0Relevant academic research and scientific papers

Preparation and Properties of Tertiary p-Alkylarylphosphines containing Straight-chain Alkyl Groups

Franks, Stephen,Hartley, Frank R.

, p. 2233 - 2237 (2007/10/02)

A series of tris(p-alkylaryl)phosphines with straight-chain alkyl groups, P(p-C6H4-CnH2n+1)3 where n=2-9, have been prepared by reaction of phosphorus trichloride with the Grignard reagent derived from the corresponding p-bromoalkylbenzene.When n=2 and 3 the phosphines are crystalline solids, but for n>3 they are viscous oils up to n=9, which is a waxy solid.The phosphines have been characterised by microanalysis, and i.r., 1H and 31P n.m.r., and mass spectrometry.The p-substituted-arylphosphines are more sensitive than triphenylphosphine to air; aerial oxidation converts them exclusively into the corresponding phosphine oxides, in contrast to trialkylphosphines which are oxidised to a complex mixture of products.The complexing ability of the new phosphines (PAr3) is demonstrated by their ready displacement of 1,5-cyclo-octadiene (cod) from (M=Pd and Pt) to yield trans- and cis-, respectively.

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