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

82363-89-1

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82363-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82363-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,6 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82363-89:
(7*8)+(6*2)+(5*3)+(4*6)+(3*3)+(2*8)+(1*9)=141
141 % 10 = 1
So 82363-89-1 is a valid CAS Registry Number.

82363-89-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-diphenylphosphanyl-1-phenylethanone

1.2 Other means of identification

Product number -
Other names phenacyldiphenylphosphine

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:82363-89-1 SDS

82363-89-1Relevant 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

Complexes of Functional Phosphines. Part 11. β-Ketophosphine Complexes of Nickel, Palladium, and Platinum. Crystal Structures of trans-

Braunstein, Pierre,Matt, Dominique,Nobel, Dominique,Balegroune, Fadila,Bouaoud, Salah-Eddine,et al.

, p. 353 - 362 (2007/10/02)

The synthesis and spectroscopic properties (1H and 31P n.m.r., i.r.) of complexes containing the β-ketophosphine Ph2PCH2C(O)Ph (HL) are described.In , (4), (5), and 2> (6), HL behaves as a P-bonded monodentate ligand whereas in the cationic complexes 2 and 2>2 it acts as a P, O chelate.The crystal structures of (1) and (3) have been determined using single-crystal X-ray diffraction methods.Compound (1) crystallises in space group P21/n, with a=10.079(3), b=11.510(3), c=15.411(3) Angstroem, β=93.42(2) deg, and Z=2.Compoumd (3) crystallises in space group P21/c, with a=9.283(1), b=10.261(1), c=19.318(1) Angstroem, β=96.20(1) deg, and Z=2.The structures have been refined to R 0.050 (R' 0.060) for (1) and to R 0.032 (R' 0.041) for (3).The geometries of these complexes are essentially identical although the ν(CO) frequencies of these complexes are significantly different -1 for (1) and 1 620 cm-1 for (3)>; the nickel atom occupies a centre of symmetry and has thus a square-planar environment.Although the ketone group is bent towards the nickel atom, no significant Ni-O bonding interaction occurs, as deduced from the Ni-O distances .In refluxing toluene (1), (4), or (5) lead to the phosphine-phosphinite complexes cis- (M=Ni, Pd, or Pt).Treatment of (1), (4), or (5) with base gives the enolato-complexes cis- (M=Ni, Pd, or Pt).Reaction of (6) with NaH affords the binuclear complex .The latter reacts with PPh3 to give cis-, and with Ph2PCH2CH2PPh2-TIPF6 to give .The P-O coupling products (R=Cl or Ph) are obtained by reaction of the complex with PCl3 and PPhCl2 respectively, and shown to have a five-co-ordinate structure.The square-planar P,P,P complex results from reaction of with TIPF6.

Synthesis of β-Diphenylphosphine-carbonyl Compounds by Reaction of Bromomethyl-carbonyl Compounds with Diphenyl(trimethylsilyl)phosphine

Brunner, Henri,Dylla, Monika E.,Hecht, Gabriele A. M.,Pieronczyk, Willigis

, p. 404 - 406 (2007/10/02)

1-Diphenylphosphinopropan-2-on-hydrobromide (1a), 2-Diphenylphosphino-1-phenylethan-1-on-hydrobromide (2a), and 1,3-Bis(diphenylphosphino)propan-2-on-bis(hydrobromide) (3a) were prepared by the reaction of the corresponding β-bromo-ketones with diphenyl(t

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