1663-35-0

Basic information

• Product Name: 2-METHOXYETHYL VINYL ETHER
• Synonyms: (2-methoxyethoxy)-ethen;1-(2-Methoxyethoxy)ethylene;1-methoxy-2-(vinyloxy)-ethan;1-Methoxy-2-(vinyloxy)ethane;1-methoxy-2-vinyloxyethane;2-Methoxyethyl ethenyl ether;2-methoxyethylethenylether;CH3OCH2CH2OCH=CH2
• CAS NO: 1663-35-0
• Molecular Formula: C₅H₁₀O₂
• Molecular Weight: 102.13
• Product Categories: monomer
• Mol File: 1663-35-0.mol
• Article Data: 11

Chemical Properties

• Melting Point: -82.7°C
• Boiling Point: 108.35°C (estimate)
• Flash Point: 9.3°C
• Appearance: /
• Density: 0.8970
• Vapor Pressure: 40.7mmHg at 25°C
• Refractive Index: 1.4300 (estimate)
• CAS DataBase Reference: 2-METHOXYETHYL VINYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHOXYETHYL VINYL ETHER(1663-35-0)
• EPA Substance Registry System: 2-METHOXYETHYL VINYL ETHER(1663-35-0)

Safety Data

• Hazardous Substances Data: 1663-35-0(Hazardous Substances Data)

Usage

General Description

2-Methoxyethyl vinyl ether, also known as 2-Methoxyethyl ethenyl ether, is a colorless liquid organic compound with the chemical formula C5H10O2. It is commonly used as a solvent for various resins, polymers, and adhesives. This chemical is also utilized in the production of synthetic polymers and as a reagent in chemical reactions. It is considered to have low toxicity but should be handled with caution as it can cause irritation to the skin, eyes, and respiratory system, and may also be harmful if ingested or inhaled in high concentrations. Additionally, it is flammable and should be stored and handled accordingly.

InChI:InChI=1/C5H10O2/c1-3-7-5-4-6-2/h3H,1,4-5H2,2H3

Upstream product

• 109-86-4 2-methoxy-ethanol 
• 1118-98-5 (1-butoxy-ethoxy)-ethene 
• 111-96-6 diethylene glycol dimethyl ether 
• 77569-95-0 2-chloroethyl diazoacetate 
• 74-86-2 acetylene 
• 74-88-4 methyl iodide 
• 143-24-8 Tetraethylene glycol dimethyl ether 
• 3315-60-4 methanolate 
• 109-92-2 ethyl vinyl ether 
• 108-31-6 maleic anhydride 
• 764-48-7 ethyleneglycol vinyl ether 
• 67-56-1 methanol 

Relevant articles and documents

Highly selective reduction of acyclic β-alkoxy ketones to protected syn-1,3-diols

(Chemical Equation Presented) The conversion of 1-(2-methoxyethoxy)ethyl- protected β-hydroxy ketones to syn-1,3-ethylidene acetals is effected by Et3SiH and SnCl4. This reaction is proposed to proceed via a cyclic oxocarbenium ion i

Vinylation of hydroxy-containing cyclic formaldehyde acetals with acetylene

Nucleophilic addition of alcohols having cyclic acetal fragments to acetylene smoothly occurs under relatively mild conditions (KOH, 100-125°C, 1-2 h, initial acetylene pressure 11-12 atm) to give the corresponding vinyl ethers in 80-83% yield.

Influence of Boiling on the Radiolysis of Diglyme

The radiolysis of diethylene glycol dimethyl ether (diglyme) in a boiling state has been studied for the first time. Boiling facilitates the cleavage of internal C–O bonds, weakens the cage effect and diglyme regeneration processes, and facilitates the exchange and dimerization reactions of radicals. As compared with radiolysis at room temperature, the amount of unsaturated products of diglyme fragmentation formed during irradiation in the boiling state is smaller by a factor of 4, and the disproportionation products of heavy radicals are found in negligible amounts, if any. The yield of radiolytic decomposition of diglyme under boiling conditions is ～15 molecule/100 eV, which is higher than that at room temperature by a factor of almost 1.5.

PROCESS FOR THE CONVERSION OF SUGARS TO LACTIC ACID AND 2-HYDROXY-3-BUTENOIC ACID OR ESTERS THEREOF COMPRISING A METALLO-SILICATE MATERIAL AND A METAL ION

The present invention regards metallo-silicate materials comprising a metal ion selected from one or more of the group consisting of potassium ions, sodium ions, lithium ions, rubidium ions and caesium ions. The materials are useful preparing lactic acid and 2-hydroxy-3-butenoic acid or esters thereof from a sugar.