(1-Ethoxycarbonylethyl)triphenylphosphonium bromide, 97%
(1-Ethoxycarbonylethyl)triphenylphosphonium bromide, 97%
(1-Ethoxycarbonylethyl)triphenylphosphonium bromide, 97%
Thermo Scientific Chemicals

(1-Ethoxycarbonylethyl)triphenylphosphonium bromide, 97%

CAS: 30018-16-7 | C23H24BrO2P | 443.32 g/mol
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100 g
Catalog number A13023.22
also known as A13023-22
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Quantity:
100 g
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Price (USD)
150.65
Online Exclusive
167.00
Save 16.35 (10%)
Each
Chemical Identifiers
CAS30018-16-7
IUPAC Name(1-ethoxy-1-oxopropan-2-yl)triphenylphosphanium bromide
Molecular FormulaC23H24BrO2P
InChI KeyRSYXORMKBUFAMS-UHFFFAOYNA-M
SMILES[Br-].CCOC(=O)C(C)[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
FormCrystals or powder or crystalline powder
Assay (Titration ex Bromide)≥96.0 to ≤104.0%
Water Content (Karl Fischer Titration)≤1.5%
Appearance (Color)White to pale cream
1-Ethoxycarbonylethyl)triphenylphosphonium bromide is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is widely used as an organophosphine catalyst.

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
1-Ethoxycarbonylethyl)triphenylphosphonium bromide is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is widely used as an organophosphine catalyst.

Solubility
Soluble in water.

Notes
Hygroscopic. Moisture sensitive. Incompatible to strong oxidizing agents. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Stable under recommended storage conditions.
RUO – Research Use Only

General References:

  1. T Fujimoto.; Y Kodama.; I Yamamoto. Synthesis of Seven-Membered Cyclic Enol Ether Derivatives from the Reaction of a Cyclic Phosphonium Ylide with α, β-Unsaturated Esters. Bioorganic & medicinal chemistry. 199762 (19), 6627-6630.
  2. H El Sayed.; HA Hamid.; AA Kassem.; M Shoukry. Synthesis and Reactions of Acenaphthenequinones-Part-2. The Reactions of Acenaphthenequinones. Molecules. 20027 (2), 155-188.