80392-30-9

Basic information

• Product Name: Benzene, [2-(2-methoxyethoxy)ethoxy]-
• CAS NO: 80392-30-9
• Molecular Formula: C11H16O3
• Molecular Weight: 196.246
• Mol File: 80392-30-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, [2-(2-methoxyethoxy)ethoxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [2-(2-methoxyethoxy)ethoxy]-(80392-30-9)
• EPA Substance Registry System: Benzene, [2-(2-methoxyethoxy)ethoxy]-(80392-30-9)

Safety Data

• Hazardous Substances Data: 80392-30-9(Hazardous Substances Data)

Upstream product

• 104-68-7 2-(2-phenoxyethoxy)ethanol 
• 74-88-4 methyl iodide 
• 20485-44-3 2,3-dimethyl-2,3-diaminobutane 
• 54149-17-6 2-bromoethyl 2-methoxyethyl ether 
• 108-95-2 phenol 
• 139-02-6 sodium phenoxide 
• 2243-44-9 2-(2-phenoxyethoxy)ethyl chloride 
• 111-77-3 2-(2-methoxyethoxy)ethyl alcohol 
• 62-53-3 aniline 

Downstream Products

• 1379476-09-1 tris(4-(2-(2-methoxyethoxy)ethoxy)phenyl)sulfonium 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate 
• 112968-89-5 1-bromo-4-[2-(2-methoxyethoxy)ethoxy]benzene 
• 929259-36-9 1-bromo-2-[2-(2-methoxyethoxy)ethoxy]benzene 

Relevant articles and documents

IODONIUM SALT COMPOUND, PHOTOACID GENERATOR AND COMPOSITION CONTAINING THE SAME, AND METHOD FOR MANUFACTURING DEVICE

PROBLEM TO BE SOLVED: To provide an iodonium salt compound which can be used as a chemical amplification type photoacid generator for resist and a photocationic polymerization initiator, has high sensitivity to an i-line at a wavelength of 365 nm, and has high solubility to an organic solvent and a resin. SOLUTION: A new iodonium salt compound is represented by the following iodonium salts 2, 5 and 10. SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2019,JPOandINPIT

Diazotisation of aromatic amines and solvolysis of diazonium salts in ethylene glycol ethers

Aniline and unhindered alkyl-substituted anilines undergo solvolysis in dioxane and DME saturated with dry hydrogen chloride on diazotisation with isoamyl nitrite to give 2-(2-chloroethoxy)ethyl aryl ethers and 2-methoxyethyl aryl ethers respectively in 36-47% yields. 2,6-Dialkyl-substituted anilines give the corresponding chloro compounds as the major product along with the aryl ethers in lower yields. Diazotisation of aniline in ethylene glycol and monomethyl ethers of ethylene glycol and diethylene glycol gave the corresponding alcoholysis products in low yields. The solvolysis of aniline did not occur on diazotisation in diethyl ether or THF.