(4-Methoxybenzyl)triphenylphosphonium chloride

(4-Methoxybenzyl)triphenylphosphonium chloride - Names and Identifiers

Name	(4-Methoxybenzyl)triphenylphosphonium chloride
Synonyms	4-METHOXYBENZYLTRIPHENYLPHOSPHONIUM CHLO (P-METHOXYBENZYL)TRIPHENYLPHOSPHONIUM CHLORIDE (4-Methoxybenzyl)triphenylphosphonium chloride (4-METHOXYBENZYL)TRIPHENYLPHOSPHONIUM CHLORIDE [(4-Methoxyphenyl)methyl]triphenylphosphonium Chloride
CAS	3462-97-3

(4-Methoxybenzyl)triphenylphosphonium chloride - Physico-chemical Properties

Molecular Formula	C26H24ClOP
Molar Mass	418.89
Melting Point	236-238°C
Appearance	Powder
Color	White
BRN	4173378
Storage Condition	Store below +30°C.
MDL	MFCD00031572

(4-Methoxybenzyl)triphenylphosphonium chloride - Risk and Safety

Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing.
WGK Germany	WGK 3 highly water e
HS Code	29310099

(4-Methoxybenzyl)triphenylphosphonium chloride - Introduction

(4-Methoxybenzyl)triphenylphosphonium chloride (also known as 4-Methoxybenzyl)triphenylphosphonium chloride) is an organic compound. The following is a description of its nature, use, formulation and safety information:

Nature:
-Appearance: White to light yellow solid
-Molecular formula: C27H27ClOP
-Molecular weight: 428.95g/mol
-melting point: 182-184°C

Use:
(4-Methoxybenzyl)triphenylphosphonium chloride are widely used in the field of organic synthesis:
-As a catalyst: it can be used as a catalyst for olefin conversion reaction, catalytic cyclization reaction, etc.
-as a crosslinking reagent: it can react with ethers and esters to form crosslinking compounds, which are used to prepare high molecular polymers, resins and coatings.

Preparation Method:
(4-Methoxybenzyl) The synthesis of triphenylphosphonium chloride is usually through the following steps:
1. with triphenylphosphine as starting material, reaction with benzylidene chloride (benzylidene) triphenylphosphine chloride.
2. reacting (benzylidene) triphenylphosphine chloride with methanol to generate (4-Methoxybenzyl)triphenylphosphonium chloride.

Safety Information:
Since the (4-Methoxybenzyl)triphenylphosphonium chloride has not been widely studied, its detailed security information may be limited. However, in general, phosphine chloride-based compounds may be potentially hazardous and toxic, requiring the following precautions in operation:
-Need to wear appropriate personal protective equipment, such as lab gloves, protective glasses and lab coats.
-Avoid inhalation, ingestion and skin contact. In case of accidental contact, rinse immediately with plenty of water and seek medical help.
-When handling the compound, it is recommended to do it in a well-ventilated laboratory environment and strictly follow the safe operating procedures.

In view of the complexity of chemicals, please make sure to conduct a detailed study of the relevant literature before use and handling, and consult a chemical professional if necessary.

Last Update：2024-04-10 22:29:15