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Diphenylcyanophosphine, also known as (diphenylphosphino)acetonitrile, is an organophosphorus compound with the chemical formula C13H10NP. It is a colorless to pale yellow crystalline solid that is soluble in organic solvents. diphenylcyanophosphine is primarily used as a ligand in coordination chemistry, particularly in the formation of transition metal complexes. It is also employed as a reagent in organic synthesis, where it can act as a phosphine source or a cyanide donor. Diphenylcyanophosphine is known for its stability and its ability to form stable complexes with various metal ions, making it a valuable tool in the field of inorganic and organometallic chemistry.

4791-48-4

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4791-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4791-48-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,9 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4791-48:
(6*4)+(5*7)+(4*9)+(3*1)+(2*4)+(1*8)=114
114 % 10 = 4
So 4791-48-4 is a valid CAS Registry Number.

4791-48-4SDS

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 diphenylphosphinous cyanide

1.2 Other means of identification

Product number -
Other names cyanodiphenylphosphane

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:4791-48-4 SDS

4791-48-4Relevant academic research and scientific papers

Degradation of (PhP)5 by Cyanide: Formation, Structure, and Reactions of the Phenyl Cyanophosphide Ion

Schmidpeter, Alfred,Zirzow, Karl-Heinz,Burget, Guenther,Huttner, Gottfried,Jibril, Ibrahim

, p. 1695 - 1706 (2007/10/02)

Phenyl cyanophosphide PhPCN- is formed in the ractions of P(CN)2- with phenyllithium and of PhP(CN)2 with CN-, and it may be prepared by nucleophilic degradation of (PhP)5 with ammonium or phosphonium cyanides.With sulfur it yields phenyl cyanodithiophosphinates 4, by alkylation alkyl(phenyl)cyanophosphanes 6 and by hydrolysis of the latter alkyl(phenyl)phosphine oxides 7. - The molecular structure of PhPCN (3c) as determined by X-ray analysis shows an almost planar anion with 102 deg CPC angle.A long PC and short CN bond in the PCN group make PhPCN- appear as "cyanide complex of phenylphosphinidene".

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