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  8. Ethyltriphenylphosphonium bromide, 98+%, Thermo Scientific Chemicals

Ethyltriphenylphosphonium bromide, 98+%, Thermo Scientific Chemicals

Catalog Number p-7026837
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Quantity:
25 g
100 g
500 g
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1530-32-1
C20H20BrP
371.26
MFCD00011838
JHYNXXDQQHTCHJ-UHFFFAOYSA-M
ethyltriphenylphosphonium bromide, ethyl triphenyl phosphonium bromide, triphenylethylphosphonium bromide, phosphonium, ethyltriphenyl-, bromide, ethyltriphenylphosphanium bromide, ethyl triphenylphosphonium bromide, unii-r85v84ul5v, ethyltriphenylphosphoniumbromide, guaifenesin powder, pubchem18705
73727
[Br-].CC[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
This item is not returnable. View return policy
1530-32-1
C20H20BrP
371.26
MFCD00011838
JHYNXXDQQHTCHJ-UHFFFAOYSA-M
ethyltriphenylphosphonium bromide, ethyl triphenyl phosphonium bromide, triphenylethylphosphonium bromide, phosphonium, ethyltriphenyl-, bromide, ethyltriphenylphosphanium bromide, ethyl triphenylphosphonium bromide, unii-r85v84ul5v, ethyltriphenylphosphoniumbromide, guaifenesin powder, pubchem18705
73727
[Br-].CC[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1

Description

Ethyltriphenylphosphonium bromide acts as a reactant in the synthesis of D-amino acids from L-cysteine-derived thiazolidines, Leiodolide A through aldol reactions and Horner-Wadsworth-Emmons olefination. It is also used in the preparation of cycloalkanoindolines through diastereoselective intramolecular inimo-ene reactions. Further, it is used as a reagent in solid-state metathesis polycondensation to prepare alkyl-dipropenylthiophene monomers and Mizoroki-Heck cyclization and cascading Tsuji-Trost cyclization reactions.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Ethyltriphenylphosphonium bromide acts as a reactant in the synthesis of D-amino acids from L-cysteine-derived thiazolidines, Leiodolide A through aldol reactions and Horner-Wadsworth-Emmons olefination. It is also used in the preparation of cycloalkanoindolines through diastereoselective intramolecular inimo-ene reactions. Further, it is used as a reagent in solid-state metathesis polycondensation to prepare alkyl-dipropenylthiophene monomers and Mizoroki-Heck cyclization and cascading Tsuji-Trost cyclization reactions.

Solubility
Soluble in methanol. Slightly soluble in water, acetone and isopropanol.

Notes
Hygroscopic. Incompatible with oxidizing agents.
TRUSTED_SUSTAINABILITY
Melting Point 206°C to 210°C
Flash Point >200°C (392°F)
Odor Odorless
Linear Formula CH3CH2P(C6H5)3Br
Quantity 25 g
UN Number UN3077
Beilstein 3599630
Sensitivity Hygroscopic
Solubility Information Soluble in methanol. Slightly soluble in water,acetone and isopropanol.
IUPAC Name ethyl(triphenyl)phosphanium;bromide
Formula Weight 371.26
Percent Purity ≥98%
Chemical Name or Material Ethyltriphenylphosphonium bromide
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