53219-99-1

Basic information

• Product Name: 1,2-BIS(2-CHLOROETHOXY)BENZENE
• Synonyms: 1,2-BIS(2-CHLOROETHOXY)BENZENE
• CAS NO: 53219-99-1
• Molecular Formula: C₁₀H₁₂Cl₂O₂
• Molecular Weight: 235.11
• Mol File: 53219-99-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-BIS(2-CHLOROETHOXY)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-BIS(2-CHLOROETHOXY)BENZENE(53219-99-1)
• EPA Substance Registry System: 1,2-BIS(2-CHLOROETHOXY)BENZENE(53219-99-1)

Safety Data

• Hazardous Substances Data: 53219-99-1(Hazardous Substances Data)

Upstream product

• 120-80-9 benzene-1,2-diol 

Downstream Products

• 132063-20-8 4,4'-<1,2-phenylenebis(oxyethyleneoxy)>diphenol dibenzyl ether 
• 97916-49-9 4-nitro-1,2-bis(2-chloroethoxy)benzene 
• 36080-66-7 8,19-dibenzyl-6,7,9,10,17,18,20,21-octahydrodibenzo-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane 
• 164790-30-1 4,5-bis-(2'-chloroethoxy)-2-hydroxy-benzaldehyde 
• 132063-21-9 3,3'-<1,2-phenylenebis(oxyethyleneoxy)>diphenol 
• 132063-22-0 4,4'-<1,2-phenylenebis(oxyethyleneoxy)>diphenol 
• 83563-41-1 2-(2-{2-[2-(Quinolin-8-yloxy)-ethoxy]-phenoxy}-ethoxy)-benzoic acid 
• 151018-76-7 N,N'-<1,2-Phenylenbis(oxy)-2,1-ethandiyloxy-2,1-phenylen>bismethansulfonamid 
• 151018-75-6 2,2'-<1,2-Phenylenbis(oxy)-2,1-ethandiyloxy>bisanilin 
• 124804-83-7 1,2-bis(2-iodoethoxy)-4-nitrobenzene 
• 332837-14-6 1,2-bis-(2-chloro-ethoxy)-4-diethoxymethyl-benzene 
• 332837-15-7 3,4-bis(2-iodoethoxy)benzaldehyde 
• 164790-28-7 3,4-bis(2-chloroethoxy)benzaldehyde 
• 170026-25-2 3,4-di(2'-chloroethoxy)bromobenzene 

Relevant articles and documents

Two cyclotriveratrylene metal-organic frameworks as effective catalysts for Knoevenagel condensation and CO2 cycloaddition with epoxides

By using a novel imidazole-functional cyclotriveratrylene ligand, two isostructural frameworks, [Cd3(HECTV)(bdc)3]·DMF·6H2O (1) and [Zn3(HECTV)(OH-bdc)3]·3DMF·4H2O (2) (HECTV = 5,6,12,13,19

Azo and azoxythiacrown ethers: Synthesis and properties

A series of 16- and 18-membered azo- and azoxythiacrown ethers have been synthesized by reductive macrocyclization of the respective bis(nitrophenoxy) oxaalkanes. The aromatic residues located in the polyether region of the molecule were introduced to mac