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Phosphonium, triphenyl[phenyl(trimethylsilyl)methyl]-, iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144189-84-4

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144189-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144189-84-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,1,8 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 144189-84:
(8*1)+(7*4)+(6*4)+(5*1)+(4*8)+(3*9)+(2*8)+(1*4)=144
144 % 10 = 4
So 144189-84-4 is a valid CAS Registry Number.

144189-84-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenyl(phenyl(trimethylsilyl)methyl)phosphonium iodide

1.2 Other means of identification

Product number -
Other names -

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:144189-84-4 SDS

144189-84-4Relevant academic research and scientific papers

Ylide-Stabilized Phosphenium Cations: Impact of the Substitution Pattern on the Coordination Chemistry

Stalder, Tobias,Krischer, Felix,Steinert, Henning,Neigenfind, Philipp,Gessner, Viktoria H.

, (2022/01/11)

Although N-heterocyclic phosphenium (NHP) cations have received considerable research interest due to their application in organocatalysis, including asymmetric synthesis, phosphenium cations with other substitution patterns have hardly been explored. Her

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.

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