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

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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.

MANUFACTURING METHOD OF 2-METHOXYETHYL VINYL ETHER

PROBLEM TO BE SOLVED: To provide a method for manufacturing method of 2-methoxy ethyl vinyl ether at high purity and efficiently. SOLUTION: There is provided a manufacturing method of 2-methoxy ethyl vinyl ether by reacting acethylene and methylcellosolve in a reaction liquid containing a base, the reaction temperature is 90 to 130°C, the acethylene and methylcellosolve are supplied continuously or intermittently to the reaction liquid and reacted while conducting extraction of the reaction fraction. SELECTED DRAWING: Figure 2 COPYRIGHT: (C)2018,JPOandINPIT

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.