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Z-diphenyl(styryl)phosphane is an organophosphorus compound characterized by its molecular formula C17H15P. It features a phosphorus atom bonded to two phenyl groups and a styryl group, which is a vinyl group attached to a benzene ring. This chemical is known for its potential applications in organic synthesis, particularly as a ligand in transition metal-catalyzed reactions, and as a reagent in the formation of phosphorus-containing compounds. Its structure contributes to its unique reactivity and selectivity in chemical transformations, making it a valuable tool in the field of chemistry.

31239-70-0

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31239-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31239-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,3 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31239-70:
(7*3)+(6*1)+(5*2)+(4*3)+(3*9)+(2*7)+(1*0)=90
90 % 10 = 0
So 31239-70-0 is a valid CAS Registry Number.

31239-70-0Downstream Products

31239-70-0Relevant academic research and scientific papers

A bench-stable copper photocatalyst for the rapid hydrophosphination of activated and unactivated alkenes

Dannenberg, Steven G.,Waterman, Rory

supporting information, p. 14219 - 14222 (2020/11/24)

Cu(acac)2 (1) is a highly active catalyst for the hydrophosphination of alkenes. Photocatalytic conditions are critical, and provide high conversions with unactivated substrates that have never before been reported with an air-stable catalyst or at ambient temperature. The commercial availability, ease of use, and broad substrate scope of compound 1 make hydrophosphination more available to synthetic chemists.

1,1-Diphosphines and divinylphosphines via base catalyzed hydrophosphination

Coles,Mahon,Webster

supporting information, p. 10443 - 10446 (2018/09/21)

A catalytic hydrophosphination route to 1,1-diphosphines is yet to be reported: these narrow bite angle pro-ligands have been used to great effect as ligands in homogeneous catalysis. We herein demonstrate that terminal alkynes readily undergo double hydrophosphination with HPPh2 and catalytic potassium hexamethyldisilazane (KHMDS) to generate 1,1-diphosphines. A change to H2PPh leads to the formation of P,P-divinyl phosphines.

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