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Phosphorane, triphenyl[1-(trimethylsilyl)ethylidene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82294-33-5

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82294-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82294-33-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,9 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82294-33:
(7*8)+(6*2)+(5*2)+(4*9)+(3*4)+(2*3)+(1*3)=135
135 % 10 = 5
So 82294-33-5 is a valid CAS Registry Number.

82294-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenyl(1-trimethylsilylethylidene)-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names 1-trimethylsilyl ethylene triphenylphosphorane

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:82294-33-5 SDS

82294-33-5Relevant academic research and scientific papers

Synthesis and reactions of [1-(trialkylsilyl)alkylidene]triphenylphosphoranes

Bestmann,Bomhard,Dostalek,Pichl,Riemer,Zimmermann

, p. 787 - 792 (2007/10/02)

Alkylidenetriphenylphosphoranes 1 react with trialkyl halosilanes 2 to afford silylated alkylidenephosphoranes 5, which can be converted to acylated alkylidenephosphoranes 8 and 10 by trimethylsilyl carboxylates 6 or carboxylic anhydrides 10. Bis(acylalkylidenephosphoranes) 13-15 are available from 5 and bis(trimethylsilyl) dicarboxylates 12 or cyclic or polymeric anhydrides 16, 17.

Spontaneous dissociation of phosphoniumylidyl-chlorophosphines to ionic phosphenium chlorides

Schmidpeter, Alfred,Jochem, Georg

, p. 471 - 474 (2007/10/02)

The products from the replacement of two chlorofunctions of PCl3 by a pair of phosphoniumylidyl substituents or by both a phosphoniumylidyl and an amino substituent are ionic phosphenium chlorides and not covalent chlorophosphines.

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