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2-羧乙基三苯基溴化L

(2-Carboxyethyl)triphenylphosphonium bromide

CAS: 51114-94-4

Molecular Formula: C21H20BrO2P

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2-羧乙基三苯基溴化L - Names and Identifiers

Name (2-Carboxyethyl)triphenylphosphonium bromide
Synonyms CET
(2-Carboxyethyl)tri
2-Carboxyethyl triphenylphosponium bromide
2-Carobxyethyl triphenylphosphonium bromide
(2-Carboxyethyl)triphenylphosphonium bromide
(2-CARBOXYETHYL)TRIPHENYLPHOSPHONIUM BROMIDE
(2-Carboxyethyl)(triphenyl)phosphonium bromide
CAS 51114-94-4
InChI InChI=1/C21H19O2P.BrH/c22-21(23)16-17-24(18-10-4-1-5-11-18,19-12-6-2-7-13-19)20-14-8-3-9-15-20;/h1-15H,16-17H2;1H

2-羧乙基三苯基溴化L - Physico-chemical Properties

Molecular FormulaC21H20BrO2P
Molar Mass415.26
Melting Point186 °C
AppearancePowder or Chunks
ColorWhite to slightly yellow
Storage ConditionInert atmosphere,Room Temperature

2-羧乙基三苯基溴化L - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk Codes36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS37/39 - Wear suitable gloves and eye/face protection
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
HS Code29319090

2-羧乙基三苯基溴化L - Introduction

(2-Carboxyethyl)triphenylphosphonium bromide is an organic compound with the chemical formula C24H21BrP.

Nature:
(2-Carboxyethyl)triphenylphosphonium bromide is a colorless to pale yellow crystalline solid with good solubility. It is insoluble in water, but can be dissolved in organic solvents such as chloroform, ethanol and ether.

Use:
(2-Carboxyethyl)triphenylphosphonium bromide is commonly used in organic synthesis reaction of phosphating reaction. It can be used as a phosphorus source to participate in Staudinger reaction, phosphating reaction and Wittig reaction. It can also be used as a ligand for organometallic catalysts.

Preparation Method:
(2-Carboxyethyl)triphenylphosphonium bromide can be obtained by reacting triphenylphosphonium bromide with a carboxyethyl alkyl halide. First, carboxyethyl dimethyl sulfoxide is produced by the reaction of iodobromoacetic acid and dimethyl sulfoxide. Triphenylphosphonium bromide and carboxyethyl dimethyl sulfoxide are then reacted under basic conditions to produce the desired product.

Safety Information:
(2-Carboxyethyl)triphenylphosphonium bromide has low toxicity under general conditions, but it still needs to comply with routine laboratory safety operations. Avoid skin contact, eye contact and inhalation. Operate in a well-ventilated area and wear suitable personal protective equipment. In case of accidental contact, rinse the affected area immediately with plenty of water and seek medical advice.
Last Update:2024-04-10 22:29:15
2-羧乙基三苯基溴化L
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