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Diphosphine, 1,2-diphenyl-1,2-bis(trimethylsilyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51470-91-8

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51470-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51470-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,7 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51470-91:
(7*5)+(6*1)+(5*4)+(4*7)+(3*0)+(2*9)+(1*1)=108
108 % 10 = 8
So 51470-91-8 is a valid CAS Registry Number.

51470-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Diphenyl-1,2-bis(trimethylsilyl)diphosphan

1.2 Other means of identification

Product number -
Other names 1.2-Diphenyl-1.2-bis(trimethylsilyl)diphosphan

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:51470-91-8 SDS

51470-91-8Relevant academic research and scientific papers

A simple straightforward synthesis of phenylphosphane and the photoinitiator bis(mesitoyl)phenylphosphane oxide (IRGACURE 819)

Gruetzmacher, Hansjoerg,Geier, Jens,Stein, Daniel,Ott, Timo,Schoenberg, Hartmut,Sommerlade, Reinhard H.,Boulmaaz, Souad,Wolf, Jean-Pierre,Murer, Peter,Ulrich, Thomas

, p. 18 - 22 (2008/09/19)

A straightforward high-yield synthesis for the photoinitiator bis(2,4,6-trimethylbenzoyl)phenylphosphane oxide (16, IRGACURE 819) involves: i) the reaction of phenyldichlorophosphane, PhPCl2, with sodium to give [Na2(P2Ph2)(tmeda)]6 (5); ii) protonation of 5 with tert-butanol to give 1,2-diphenyldiphosphane, PhHP-PHPh (12); iii) reduction of 12 by sodium to yield [Na(PHPh)x (13); iv) protonation of 13 with tert-butanol to give phenylphosphane PhPH2 (14) in excellent yields; v) reaction of 14 with 2,4,6-trimethylbenzoylchloride (MesCOCI) in presence of the NaOt-Bu formed in steps ii and iv to give bis(2,4,6-trimethylbenzoyl)phenylphosphane 7; vi) oxygenation of 7 with 30% aqueous hydrogen peroxide to give the final product 16. This reaction can be performed in toluene with about 4 vol-% of tmeda as an activator in a one-pot synthesis without changing the solvent. The structures determined by X-ray diffraction of the unique hexameric aggregate 5 and 16 are reported. Schweizerische Chemische Gesellschaft.

PROCESS FOR THE SYNTHESIS OF CYCLOORGANYLPHOSPHANES AND DI(ALKALI METAL/ALKALINE EARTH METAL) OLIGOPHOSPHANEDIIDES

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Page/Page column 13, (2008/06/13)

The invention relates to a process for the preparation of cycloorganylphosphanes of formula 1(R1P)n by reaction of dihalo(organyl)phosphanes of formula R1PHal2 with: a) activated zinc in an organic solvent, or w

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