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Triphenyl[(trimethylsilyl)methylidene]-λ5-phosphane is a complex organophosphorus compound characterized by a phosphorus atom bonded to three phenyl groups and a trimethylsilyl group. The trimethylsilyl group is connected to a methylene bridge, which in turn is bonded to the phosphorus atom, creating a unique structure. triphenyl[(trimethylsilyl)methylidene]-lambda~5~-phosphane is of interest in organophosphorus chemistry due to its potential applications in catalysis and as a ligand in coordination chemistry. It is synthesized through the reaction of triphenylphosphine with a suitable trimethylsilyl compound, and its properties, such as reactivity and stability, are influenced by the electron-donating nature of the trimethylsilyl group. The compound's structure and properties make it a valuable tool for studying the behavior of phosphorus in various chemical reactions and for developing new materials and catalysts.

3739-97-7

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3739-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3739-97-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,3 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3739-97:
(6*3)+(5*7)+(4*3)+(3*9)+(2*9)+(1*7)=117
117 % 10 = 7
So 3739-97-7 is a valid CAS Registry Number.

3739-97-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names triphenyl(trimethylsilylmethylidene)

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

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More Details:3739-97-7 SDS

3739-97-7Relevant academic research and scientific papers

Total synthesis of echinopines A and B: Exploiting a bioinspired late-stage intramolecular cyclopropanation

Peixoto, Philippe A.,Richard, Jean-Alexandre,Severin, Rene,Chen, David Y.-K.

supporting information; experimental part, p. 5724 - 5727 (2011/12/15)

Total synthesis of echinopine A and B have been accomplished, based on a strategy that involved two transition-metal-mediated ene-yne cycloisomerizations. A modified Pd-catalyzed enyne cycloisomerization/ intramolecular Diels-Alder cascade rendered a more

A Novel Synthesis of 4H-Chromen-4-ones via Intramolecular Wittig Reaction

Kumar, Pradeep,Bodas, Mandar S.

, p. 3821 - 3823 (2007/10/03)

formula presented The acylphosphoranes formed in a sequential manner from the reaction of the silyl ester of O-acyl(aroyl)salicylic acids and (trimethylsilyl)-methylenetriphenylphosphorane undergo intramolecular Wittig cyclization on the ester carbonyl to afford the 4H-chromen-4-ones in good to excellent yields.

Stabilized and persistent allenylketenes

Huang, Wenwei,Fang, Decai,Temple, Karen,Tidwell, Thomas T.

, p. 2832 - 2838 (2007/10/03)

Photolyses of 2,3-bis(trimethylsilyl)-substituted methylenecyclobutenones 22-26 give essentially quantitative conversion to the allenylketenes 28-32 which have been isolated as long-lived species at room temperature. As predicted by molecular orbital calc

Phenylsilyl Chalcogenides, (Phenylsilyl)amines and Related Phosphonium (Phenylsilyl)methylides

Mitzel, Norbert W.,Schier, Annette,Beruda, Holger,Schmidbaur, Hubert

, p. 1053 - 1060 (2007/10/02)

The synthesis of 1,3-diphenyldisiloxane (1) by hydrolysis of chloro(phenyl)silane is optimized, 1,3-diphenyldisilthiane (2) is made available by the reaction of H2S with PhH2SiCl and triethylamine. 1,3-Diphenyldisilselenane (3) is prepared from K2Se and P

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.

NOUVELLE SYNTHESE DE SELS D'ALCADIEN-1,3 YL PHOSPHONIUM

Plenat, Francoise

, p. 4705 - 4708 (2007/10/02)

A new synthetic route to alcadien-1,3 yl phosphonium salts is given.

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