(1-Ethoxycarbonylethyl)triphenylphosphonium bromide, 97%

Name: (1-Ethoxycarbonylethyl)triphenylphosphonium bromide, 97%
SKU: A13023.22

CAS: 30018-16-7 | C23H24BrO2P | 443.32 g/mol

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数量:

25 g

100 g

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製品番号（カタログ番号） A13023.22

または、製品番号A13023-22

価格（JPY）

数量:

100 g

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化学物質識別子

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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仕様

スペックシート

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:

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.
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.