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(4-ETHYLBENZYL)TRIPHENYLPHOSPHONIUM, with the molecular formula C29H27P, is a phosphonium salt characterized by a positively charged phosphorus atom and three phenyl groups attached to it. This chemical compound is known for its versatile applications in various fields, including organic synthesis, coordination chemistry, and drug delivery systems.

207291-53-0

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207291-53-0 Usage

Uses

Used in Organic Synthesis:
(4-ETHYLBENZYL)TRIPHENYLPHOSPHONIUM is used as a phase-transfer catalyst for facilitating the transfer of ions between immiscible phases in organic synthesis reactions. Its ability to bridge different phases enhances the efficiency and selectivity of these reactions.
Used in Coordination Chemistry:
In coordination chemistry, (4-ETHYLBENZYL)TRIPHENYLPHOSPHONIUM serves as a ligand, playing a crucial role in the formation and stabilization of metal complexes. This application is vital for the development of new materials and catalysts.
Used in Drug Delivery Systems:
(4-ETHYLBENZYL)TRIPHENYLPHOSPHONIUM has been studied for its potential applications in drug delivery systems, where it can contribute to the development of innovative and efficient drug carriers.
Used as a Precursor to Phosphine Derivatives:
Furthermore, (4-ETHYLBENZYL)TRIPHENYLPHOSPHONIUM is utilized as a precursor to phosphine derivatives, which are important building blocks in the synthesis of various pharmaceuticals, agrochemicals, and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 207291-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,2,9 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 207291-53:
(8*2)+(7*0)+(6*7)+(5*2)+(4*9)+(3*1)+(2*5)+(1*3)=120
120 % 10 = 0
So 207291-53-0 is a valid CAS Registry Number.

207291-53-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-ethylphenyl)methyl-triphenylphosphanium

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:207291-53-0 SDS

207291-53-0Relevant academic research and scientific papers

ANTIVIRAL DRUGS FOR TREATMENT OF ARENA VIRUS INFECTION

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Paragraph 0000136, (2013/08/28)

Compounds, methods and pharmaceutical compositions for treating viral infections, by administering certain compounds in therapeutically effective amounts are disclosed. Methods for preparing the compounds and methods of using the compounds and pharmaceutical compositions thereof are also disclosed. In particular, the treatment and prophylaxis of viral infections such as caused by the Arenavirus family such as Lassa fever, Argentine hemorrhagic fever, Bolivian hemorrhagic fever, and Venezuelan hemorrhagic fever

Base-induced photorearrangements from 3-styrylfurans to 2-methylnaphthalenes

Ho, Jinn-Hsuan,Lee, Tunng-Hsien,Lo, Chia-Kai,Chuang, Chao-Li

supporting information; experimental part, p. 7199 - 7201 (2012/01/05)

Irradiation of 3-(4-substituted styryl)furans in basic media yielded a series of 7-substituted-2-methylnaphthalenes, including methoxy, isopropyl, ethyl, methyl, fluoro, and cyano substituents. This base-induced photorearrangement involves cis-trans photoisomerization, 6e photocyclization, base-induced elimination, and a Norrish Type I photoreaction and is a novel method to synthesize unsymmetrical 2,7-disubstituted naphthalenes.

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