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

115140-72-2

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115140-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115140-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,4 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115140-72:
(8*1)+(7*1)+(6*5)+(5*1)+(4*4)+(3*0)+(2*7)+(1*2)=82
82 % 10 = 2
So 115140-72-2 is a valid CAS Registry Number.

115140-72-2Downstream Products

115140-72-2Relevant academic research and scientific papers

Synthesis of the phosphorus-carbon double bond by reaction between pentacarbonylchromium or -tungsten complexes of phosphinidenes and carbenes. Application to the synthesis of the 1,2-dihydrophosphete ring

Huy, Ngoc Hoa Tran,Ricard, Louis,Mathey, Fran?ois

, p. 1791 - 1795 (2008/10/08)

The condensation of a carbene complex R1R2C=M(CO)5 with a transient terminal phosphinidene complex [RP=M(CO)5] (M = Cr, W) primarily yields a phosphaalkene complex, R1R2C=P(R)→M(CO)5, which, in some cases, dimerizes. This method has been applied to the synthesis of Ph2C=P(Ph)→W(CO)5 which is stable as a monomer. When a vinylcarbene complex such as PhCH=CH-C(OEt)=Cr(CO)5 is reacted with (phenylphosphinidene)pentacarbonyltungsten, the transient phosphabutadiene complex thus obtained instantly undergoes a [2 + 2] cyclization to give a (1,2-dihydrophosphete(P-W))pentacarbonyltungsten complex. The X-ray crystal structure analysis of this complex [C22H17O6PW, fw 592.20; space group P1 (No. 2) with a = 10.519 (1) ?, b = 10.887 (1) ?, c = 11.134 (1) ?, α = 112.78 (2)°, β = 98.15 (2)°, γ = 97.13 (2)°; V = 1141.18 (68) ?3; Z = 2; d(calcd) = 1.723 g cm-3] confirms the presence of the four-membered ring with a very long P-C sp3-intracyclic bond [1.902 (5) ?]. It proved possible to convert this complex into the corresponding P-oxide without breaking the ring.

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