78830-79-2

Basic information

• Product Name: 2,4-DICHLORO-1-(2,2-DIETHOXYETHOXY)BENZENE
• Synonyms: 2,4-DICHLORO-1-(2,2-DIETHOXYETHOXY)BENZENE;2,4-DICHLOROPHENOXYACETALDEHYDE DIETHYL ACETAL;2-(2,4-DICHLOROPHENOXY)ACETALDEHYDE DIETHYLACETAL
• CAS NO: 78830-79-2
• Molecular Formula: C₁₂H₁₆Cl₂O₃
• Molecular Weight: 279.16
• Mol File: 78830-79-2.mol

Chemical Properties

• Boiling Point: 350.8°C at 760 mmHg
• Flash Point: 122.9°C
• Appearance: /
• Density: 1.198g/cm³
• Vapor Pressure: 8.65E-05mmHg at 25°C
• Refractive Index: 1.507
• CAS DataBase Reference: 2,4-DICHLORO-1-(2,2-DIETHOXYETHOXY)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-DICHLORO-1-(2,2-DIETHOXYETHOXY)BENZENE(78830-79-2)
• EPA Substance Registry System: 2,4-DICHLORO-1-(2,2-DIETHOXYETHOXY)BENZENE(78830-79-2)

Safety Data

• Hazardous Substances Data: 78830-79-2(Hazardous Substances Data)

Usage

Uses

Used in Agricultural Industry:
2,4-DICHLORO-1-(2,2-DIETHOXYETHOXY)BENZENE is used as a herbicide for controlling a wide range of weeds that can hinder crop growth and reduce agricultural productivity. Its application helps in maintaining the health and yield of crops by eliminating competing plant species.
Used in Industrial Settings:
In industrial areas where unwanted vegetation can lead to various issues such as reduced aesthetics, safety hazards, or interference with infrastructure, 2,4-DICHLORO-1-(2,2-DIETHOXYETHOXY)BENZENE is employed as a pesticide to manage and control weed growth effectively.
It is crucial to follow the guidelines and regulations for the use of 2,4-DICHLORO-1-(2,2-DIETHOXYETHOXY)BENZENE to minimize its potential impact on human health and the environment. This includes taking necessary precautions during application, storage, and disposal to ensure safety and sustainability.

InChI:InChI=1/C12H16Cl2O3/c1-3-15-12(16-4-2)8-17-11-6-5-9(13)7-10(11)14/h5-7,12H,3-4,8H2,1-2H3

Upstream product

• 2032-35-1 Bromoacetaldehyde diethyl acetal 
• 120-83-2 2,4-dichlorophenol 
• 621-62-5 chloroacetaldehyde diethyl acetal 

Downstream Products

• 78830-81-6 2-(2,4-dichlorophenoxymethyl)-4-methacryloyloxymethyl-1,3-dioxolane 
• 17944-27-3 (2,4-dichlorophenoxy)acetaldehyde 
• 17592-43-7 4-(2,4-dichloro-phenoxy)-trans-crotonic acid 
• 61756-77-2 (2,4-dichloro-phenoxy)-acetaldehyde-semicarbazone 
• 23145-06-4 5,7-dichlorobenzofuran 

Relevant articles and documents

Zeolite-catalyzed synthesis of 2,3-unsubstituted benzo[b]furans via the intramolecular cyclization of 2-aryloxyacetaldehyde acetals

An efficient and environmentally benign heterogeneous catalytic process for the synthesis of 2,3-unsubstituted benzo[b]furans has been established via the intramolecular cyclization of 2-aryloxyacetaldehyde acetals. By utilizing tin-exchanged H-β zeolite (Sn-β) as catalyst, a wide range of functionalized 2,3-unsubstituted benzo[b]furans could be prepared in good to excellent yields. The Sn-β zeolite catalyst also exhibited excellent shape selectivity on the cyclization of meta-substituted 2-aryloxyacetaldehyde acetals, and 6-substituted isomers were preferably formed up to 97% regio-selectivity. Moreover, Sn-β zeolite could be easily recovered and reused without any noticeable activity loss.

1,3-Dioxolane Bearing Perfume and Herbicide Aldehyde Residues

4-Methacryloyloxymethyl-1,3-dioxolanes substituted at the 2 position with perfume and herbicide aldehyde residues were synthesized either by acetalization or by transacetalization involving 2,3-dihydroxypropyl methacrylate.The effect of the 2-substituent of the dioxolane ring on the rate of hydrolysis was remarkable.