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Phosphonium, [(diphenylphosphino)(triphenylphosphoranylidene)methyl]triphenyl-, chloride is a complex organophosphorus compound characterized by its unique structure. It features a phosphonium cation with a central phosphorus atom bonded to three phenyl groups and a fourth bond to a methyl group. This methyl group is further connected to a diphenylphosphino group and a triphenylphosphoranylidene group, which together contribute to the molecule's stability and reactivity. The chloride anion is associated with the phosphonium cation, forming an ionic bond. Phosphonium, [(diphenylphosphino)(triphenylphosphoranylidene)methyl]triphenyl-, chloride is significant in the field of organophosphorus chemistry, potentially serving as a ligand in coordination chemistry or a precursor in the synthesis of more complex phosphorus-containing molecules. Its specific applications may include catalysis and the formation of metal-organic frameworks, although further research would be needed to explore its full potential.

7560-06-7

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7560-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7560-06-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,6 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7560-06:
(6*7)+(5*5)+(4*6)+(3*0)+(2*0)+(1*6)=97
97 % 10 = 7
So 7560-06-7 is a valid CAS Registry Number.

7560-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (Diphenylphosphino)(triphenylphosphonio)(triphenylphosphoranyliden)methan-chlorid

1.2 Other means of identification

Product number -
Other names [Diphenylphosphanyl-(triphenyl-λ5-phosphanylidene)-methyl]-triphenyl-phosphonium

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:7560-06-7 SDS

7560-06-7Relevant academic research and scientific papers

Carbodiphosphorane mediated synthesis of a triflyloxyphosphonium dication and its reactivity towards nucleophiles

Yogendra,Hennersdorf,Bauzá,Frontera,Fischer,Weigand

, p. 2954 - 2957 (2017)

A carbodiphosphorane ((Ph3P)2C) mediated synthesis of the first triflyloxyphosphonium dication (12+) bearing two electrophilic sites is presented. Depending on the nucleophile, 12+ reacts selectively either at the sulfur atom of the triflyloxy moiety or at the directly attached phosphorus atom. In substitution reactions at the phosphorus atom the triflyloxy moiety serves as a leaving group and enables the synthesis of rare examples of pseudo-halophosphonium dications.

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