6230-82-6 Usage
Description
(2-oxo-2-phenylethyl)(triphenyl)phosphonium iodide is a phosphonium salt with the molecular formula C40H31IO2P. It features a phenylethyl and triphenyl group attached to a phosphorus atom, along with an iodide ion counterion.
Uses
Used in Organic Synthesis:
(2-oxo-2-phenylethyl)(triphenyl)phosphonium iodide is used as a precursor for the synthesis of various organic and pharmaceutical compounds, contributing to the creation of a wide range of molecules with potential applications in different industries.
Used as a Catalyst in Organic Reactions:
In the field of organic chemistry, (2-oxo-2-phenylethyl)(triphenyl)phosphonium iodide serves as a catalyst, particularly for reactions that involve the formation of carbon-carbon bonds. Its use accelerates these reactions and enhances the overall efficiency of the process.
Used in Medicinal Applications:
(2-oxo-2-phenylethyl)(triphenyl)phosphonium iodide is known for its potential biological activity and is being studied for its possible use in medicinal applications. Its unique structure and properties make it a promising candidate for further research and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 6230-82-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,3 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6230-82:
(6*6)+(5*2)+(4*3)+(3*0)+(2*8)+(1*2)=76
76 % 10 = 6
So 6230-82-6 is a valid CAS Registry Number.
6230-82-6Relevant articles and documents
ALKYLATION OF ARSENIC AND PHOSPHORUS β-KETOYLIDES
Nesmeyanov, Nik. A.,Kharitonov, V. G.,Zhuzhlikova, S. T.,Petrovskii, P. V.,Antipin, M. Yu.,et al.
, p. 1417 - 1428 (2007/10/02)
The dual reactivity of a series of arsenic and phosphorus β-ketoylides in alkylation reactions and the effect of various factors on the reaction path were studied.The arsenic ketoylides were more susceptible to C-alkylation than the phosphorus ylides.In a number of cases C-alkylation was accompanied by secondary O-alkylation.The proportion of O-alkylation increases sharply in the transition from methyl iodide to methyl bromide and then to Me3O(1+)BF4(1-) and also in the series MeI, PhCH2I, EtI.The introduction of alkyl substituents at the α position greatly hinders C-alkylation.Only one of the two possible geometric isomers is always formed during the reactions at the oxygen center.X-ray crystallographic analysis of triphenyl(2-methoxy-1-propenyl)arsonium iodide showed that this compound was the Z isomer.