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1,15-bis(diphenylphosphinoyl)-2,5,8,11,14-pentaoxapentadecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132789-72-1

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132789-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132789-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,7,8 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 132789-72:
(8*1)+(7*3)+(6*2)+(5*7)+(4*8)+(3*9)+(2*7)+(1*2)=151
151 % 10 = 1
So 132789-72-1 is a valid CAS Registry Number.

132789-72-1Downstream Products

132789-72-1Relevant academic research and scientific papers

Synthesis, complexing properties, and selectivity of bis(diphenylphosphorylmethyl) ethers of oligoethylene glycols. Crystal structure of 1,3-bis(diphenylphosphoryl)-2-oxapropane

Ivanova,Baulin,Polyakova,Pyatova,Krivorot’ko,Galkina,Tsivadze, A. Yu.

, p. 2574 - 2581 (2017/12/26)

A convenient method of synthesis of phosphoryl-substituted podands with dipehnylphosphorylmethyl end groups of the general formula Ph2P(O)CH2O(CH2CH2O)nCH2P(O)Ph2 (Ln, n = 0–6) is described. The stability constants of the complexes of the podands with alkali metal 2,4-dinitrophenolates were determined by conductometry. The ion-selective properties of the podands with respect to alkali and alkaline-earth metal cations were assessed by ionometry. The crystal structure of 1,3-bis(diphenylphosphoryl)-2-oxapropane was established by X-ray diffraction analysis.

Phosphorus-containing podands: XV. Synthesis of bis(diphenylphosphinoylmethyl) ethers of oligoethylene glycols and selectivity of their complex formation with alkali metal cations in a low-polarity solvent

Tsvetkov,Evreinov,Bondarenko,Safronova

, p. 1039 - 1046 (2007/10/03)

An improved procedure for preparing bis(diphenylphosphinoylmethyl) ethers of oligoethelene glycols of the general formula Ph2P(O)CH2O(CH2CH2O)nCH 2P(O)Ph2 (n = 0-6) is developed, and the stability constants of their alkali cation complexes in the THF-CHCl3 system at 25°C were determined by conductometry.

ALKYLATION REACTIONS OF DIALKYL HYDROGEN PHOSPHITES AND DIARYLPHOSPHINE OXIDES UNDER PHASE-TRANSFER CONDITIONS

Petrov, K. A.,Sivova, L. I.,Smirnov, I. V.,Kryukova, L. Yu.

, p. 264 - 268 (2007/10/02)

It was shown that phosphonates and tertiary phosphine oxides can be synthesized by the alkylation of acid phosphites and diarylphosphine oxides in a nonpolar solvent in presence of solid potassium hydroxide and potassium carbonate and also catalytic amounts of 18-crown ether (or in its absence). (Diarylphosphinyl)methyl ethers of mono- and oligo-etylene glycols were synthesized by the reactions of diaryl(chloromethyl)phosphine oxides with lithium glycolates

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