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Triphenyl(triphenylphosphoranylidenamino)phosphonium-phenylcyanphosphid is a complex organophosphorus compound with the chemical formula C42H30NP3. It is a phosphonium salt, characterized by the presence of a positively charged phosphorus atom bonded to three phenyl groups and a triphenylphosphoranylidenamino group. The latter is a phosphorus-nitrogen double bond (P=N) that is part of a larger cyclic structure. Additionally, the compound features a phenylcyanophosphid group, which is a phenyl group bonded to a cyanide and a phosphorus atom. This molecule is of interest in organophosphorus chemistry due to its unique structure and potential applications in various chemical reactions and as a ligand in coordination chemistry.

90826-87-2

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90826-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90826-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,2 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90826-87:
(7*9)+(6*0)+(5*8)+(4*2)+(3*6)+(2*8)+(1*7)=152
152 % 10 = 2
So 90826-87-2 is a valid CAS Registry Number.

90826-87-2Downstream Products

90826-87-2Relevant 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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