19578-69-9

Basic information

• Product Name: 1-(benzyloxy)-2,4-dichlorobenzene
• Synonyms: 1-Benzyloxy-2,4-dichloro-benzene
• CAS NO: 19578-69-9
• Molecular Formula: C₁₃H₁₀Cl₂O
• Molecular Weight: 253.1239
• Mol File: 19578-69-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 349.7°C at 760 mmHg
• Flash Point: 127.4°C
• Density: 1.278g/cm³
• Vapor Pressure: 9.35E-05mmHg at 25°C
• Refractive Index: 1.594
• CAS DataBase Reference: 1-(benzyloxy)-2,4-dichlorobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(benzyloxy)-2,4-dichlorobenzene(19578-69-9)
• EPA Substance Registry System: 1-(benzyloxy)-2,4-dichlorobenzene(19578-69-9)

Safety Data

• Hazardous Substances Data: 19578-69-9(Hazardous Substances Data)

Usage

General Description

1-(benzyloxy)-2,4-dichlorobenzene, also known as benzyl 2,4-dichlorophenyl ether, is a chemical with the molecular formula C14H10Cl2O. It is a benzyl ether derivative of 2,4-dichlorophenol, and can be synthesized through the reaction of benzyl chloride and 2,4-dichlorophenol. 1-(benzyloxy)-2,4-dichlorobenzene is commonly used in the synthesis of pharmaceuticals, agrochemicals, and dyes. It has also been researched for its potential insecticidal properties. 1-(benzyloxy)-2,4-dichlorobenzene is a white solid with a high melting point and low solubility in water, making it suitable for use in various chemical reactions and applications.

Upstream product

• 3757-76-4 sodium 2,4-dichlorophenolate 
• 100-44-7 benzyl chloride 
• 120-83-2 2,4-dichlorophenol 
• 100-58-3 phenylmagnesium bromide 
• 1078-58-6 diphenylzinc 
• 94-75-7 2,4-Dichlorophenoxyacetic acid 

Downstream Products

• 190199-40-7 1-(2,4-dichlorophenyl)-1H-imidazole 

Relevant articles and documents

Redox-Active Esters in Fe-Catalyzed C-C Coupling

Cross-couplings of alkyl halides and organometallic species based on single electron transfer using Ni and Fe catalyst systems have been studied extensively, and separately, for decades. Here we demonstrate the first couplings of redox-active esters (both isolated and derived in situ from carboxylic acids) with organozinc and organomagnesium species using an Fe-based catalyst system originally developed for alkyl halides. This work is placed in context by showing a direct comparison with a Ni catalyst for >40 examples spanning a range of primary, secondary, and tertiary substrates. This new C-C coupling is scalable and sustainable, and it exhibits a number of clear advantages in several cases over its Ni-based counterpart.

PESTICIDAL SUBSTITUTED PHENYLETHERS

The invention relates to the use of phenylether derivatives of formula (I), to compositions thereof for the control of pests, including arthropods and helminths.