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Phosphine oxide, [1,2-phenylenebis(methylene)]bis[diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15303-27-2

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15303-27-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15303-27-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,0 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15303-27:
(7*1)+(6*5)+(5*3)+(4*0)+(3*3)+(2*2)+(1*7)=72
72 % 10 = 2
So 15303-27-2 is a valid CAS Registry Number.

15303-27-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-phenylene-bis(methylene)bis(diphenylphosphine oxide)

1.2 Other means of identification

Product number -
Other names o-C6H4(CH2P(O)Ph2)2

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:15303-27-2 SDS

15303-27-2Relevant academic research and scientific papers

Extraction of rare-earth elements(III) from nitric acid solutions with bis(diarylphosphorylmethyl)benzenes

Turanov,Karandashev,Baulin,Kirillov,Kirillov,Rychkov,Tsivadze

, p. 1015 - 1021 (2015)

Abstract Extraction of micro quantities of rare-earth elements(III) from HNO3 solutions as complexes with bis(diarylphosphorylmethyl)benzenes depending on the nature of organic diluent and HNO3 concentration in equilibrium aqueous ph

Synthesis method of trisubstituted phosphine oxide compound

-

Paragraph 0031, (2019/05/08)

The invention provides a synthesis method of a trisubstituted phosphine oxide compound. In the method, monohydric alcohol or dihydric alcohol which is inexpensive, readily available, stable and low intoxicity are used as alkylating agents, and cheap and readily available halosilane is used as a catalyst, thus directly obtaining the trisubstituted phosphine oxide compound through high-selectivityreaction. The reaction method is simple, the conditions are mild, no solvent is needed, the operation is easy, and water is a reaction by-product. The method has low requirements on the reaction conditions, and benzyl type, allyl type and aliphatic type alcohol can be used as the alkylating agent to realize the synthesis of the target phosphine oxide compound, and has a relatively wide applicationrange. The method can also conveniently scale up the production by 20 times and carry out the gram-level preparation of products, so the method should also have certain research and industrial application prospects.

Expedient synthesis of substituted (diphenylphosphinoylmethyl)benzenes

Bew, Sean P.,Brimage, Rebecca A.,Hughes, David L.,Legentil, Laurent,Sharma, Sunil V.,Wilson, Martin A.

, p. 2655 - 2658 (2007/10/03)

An efficient protocol for the synthesis of structurally diverse (diphenylphosphinoylmethyl)benzenes is described. The reaction employs readily available carboxylic acids, chlorodiphenylphosphine, and water as the reagents. A 97% reduction in the reaction

Tetraphenylalkylenediphosphine dioxides as extractants of palladium from nitric acid solutions

Turanov,Tsvetkov,Kharitonov,Safronova,Yarkevich

, p. 1075 - 1080 (2007/10/03)

A complete series of tetraphenyl-α,ω-alkanediyldiphosphine dioxides Ph2P(O)(CH2)nP(O)Ph2 (n = 1-10) was synthesized, and their extraction properties were studied. 1,5-Bis(diphenylphosphinoyl)pentane showed the highest extraction ability with respect to palladium. A synergistic effect was observed in the extraction of palladium with toluene solutions of 1,5-bis(diphenylphosphinoyl)pentane in the presence of tributyl phosphate.

TERTIAERE PHOSPHINOXIDE AUS DIPHENYLCHLORPHOSPHIN UND CARBONSAEUREN

Sartori, Peter,Mosler, Gerhard

, p. 115 - 120 (2007/10/02)

Starting from Diphenylchlorophosphine and mono or dicarboxylic acids, the preparation of diphenylalkylphosphine oxides, in good yields in a simple synthetic procedure is described.

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