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1-phenyl-2-(diisopropylphosphino)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76734-60-6

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76734-60-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76734-60-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,7,3 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76734-60:
(7*7)+(6*6)+(5*7)+(4*3)+(3*4)+(2*6)+(1*0)=156
156 % 10 = 6
So 76734-60-6 is a valid CAS Registry Number.

76734-60-6Relevant academic research and scientific papers

Synthesis and characterization of Co and Ni complexes stabilized by keto- and acetamide-derived P,O-type phosphine ligands

Agostinho, Magno,Rosa, Vitor,Aviles, Teresa,Welter, Richard,Braunstein, Pierre

experimental part, p. 814 - 822 (2009/06/19)

The coordination properties of the β-keto phosphine ligands R 2PCH2C(O)Ph (HL1, R = i-Pr; HL2, R = Ph), of the new acetamide-derived phosphine ligand (i-Pr)2PNHC(O)Me (HL3) and of Ph2

Coordination chemistry of a mixed donor bidentate ligand with nickel. A tetrameric enolate of sodium that binds a phosphine donor

Fryzuk, Michael D.,Gao, Xiaoliang,Rettig, Steven J.

, p. 1175 - 1180 (2007/10/03)

The preparation of a mixed donor ligand consisting of an enolate and neutral phosphine is described and its coordination chemistry with nickel reported.The phosphino ketones R2PCH2COPh (R=Cy or i-Pr) are prepared by the reaction of the corresponding secondary phosphines with bromoacetophenone to form the corresponding phosphonium salts +Br- (R=Cy or i-Pr); subsequent deprotonation leads to the neutral ketones.The enolates are formed by addition of NaN(SiMe3)2 to the neutral ketone.The crystal structure of the sodium enolate having isopropyl substituent at phosphorus displays a tetrameric structure in the soild state and there is an interaction of the phosphorus donor with the sodium anion: Na-P, 2.852(2) Angstroem.The preparation of a series of nickel complexes was achieved by addition of the sodium enolate to the appropriate Ni(II) starting material.The structures of the nickel derivatives are reported.The catalytic behaviour of one of these complexes in the polymerization and oligomerization of ethylene is briefly described.Crystals of >4, 2b, are tetragonal, a=b=20.790(2) Angstroem, c=13.539(7) Angstroem, Z=4, space group I41/a1; those of (PPh3)NiPh, 3a, are triclinic, a=10.742(2) Angstroem, b=19.811(3) Angstroem, c=10.621(2) Angstroem, α=101.88(1) deg, β=119.24(1) deg, γ=91.08(1) deg, Z=2, space group P; and those of (PPh3)NiPh, 3b, are triclinic, a=10.219(1) Angstroem, b=17.432(3) Angstroem, c=9.788(1) Angstroem, α=101.18(1) deg, β=100.19(1) deg, γ=85.32(1) deg, Z=2, space group P.The structures were solved by direct (2b) and Patterson (3a and 3b) methods and were refined by full-matrix least-squares procedures to R=0.045, 0.044, and 0.032 (RW=0.038, 0.041, and 0.030) for 965, 4483, and 5085 reflections with I>/=3?(I) respectively.Key words: nickel, sodium enolate, homogeneous catalyst, oligomerization.

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