20524-89-4

Basic information

• Product Name: 1-(-Ethoxyethoxy)-1,2-propadiene
• Synonyms: 1-(-Ethoxyethoxy)-1,2-propadiene
• CAS NO: 20524-89-4
• Molecular Formula: C₇H₁₂O₂
• Molecular Weight: 128.16898
• Mol File: 20524-89-4.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(-Ethoxyethoxy)-1,2-propadiene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(-Ethoxyethoxy)-1,2-propadiene(20524-89-4)
• EPA Substance Registry System: 1-(-Ethoxyethoxy)-1,2-propadiene(20524-89-4)

Safety Data

• Hazardous Substances Data: 20524-89-4(Hazardous Substances Data)

Usage

General Description

1-(-Ethoxyethoxy)-1,2-propadiene, also known as Ethyltriethylene glycol vinyl ether, is a chemical compound with the molecular formula C8H14O3. It is a colorless liquid with a slightly sweet odor. 1-(-Ethoxyethoxy)-1,2-propadiene is commonly used as a solvent and as a monomer in polymerization reactions. It is also used in the production of resins, coatings, and adhesives. Ethyltriethylene glycol vinyl ether has low toxicity and is not known to be harmful to the environment, making it a popular choice in various industrial applications. However, it is important to handle and store it properly to prevent any potential hazards associated with its use.

Upstream product

• 18669-04-0 acetaldehyde ethyl propargyl acetal 

Downstream Products

• 137122-53-3 Propenoyltriphenylsilane 
• 137122-57-7 1-[dimethyl(phenyl)silyl]prop-2-en-1-one 
• 700873-79-6 6-methyl-2-methylsulfanyl-5,6-dihydro-4H-pyridin-3-one 
• 137122-55-5 Diphenylpropenoylprop-1-ynyl-silane 
• 137122-42-0 [1-(1-Ethoxy-ethoxy)-propa-1,2-dienyl]-diphenyl-silane 
• 86486-53-5 [1-(1-Ethoxy-ethoxy)-3-phenylselanyl-propa-1,2-dienyl]-trimethyl-silane 

Relevant articles and documents

One-Pot Synthesis of 1-(1-Alkoxyethoxy)allenes

A convenient one-pot procedure has been proposed for the preparation of 1-(1-alkoxyethoxy)allenes from alkoxyethenes and prop-2-yn-1-ol with the use of trifluoroacetic acid as highly efficient catalyst for the synthesis of 3-(1-alkoxyethoxy)prop-1-ynes and of the system t-BuOK–DMSO for the isomerization of the latter into allenes.

[3 + 4] Annulation using a [β-(trimethylsilyl) acryloyl]silane and the lithium enolate of an α,β-unsaturated methyl ketone: (1R,6S,7S)-4-(tert- butyldimethylsiloxy)-6-(trimethylsilyl)bicyclo [5.4.0]undec-4-EN-2-one

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SILYL KETONE CHEMISTRY. PREPARATION AND REACTIONS OF UNSATURATED SILYL KETONES

A series of silyl ketones has been prepared by appropriate manipulation of α-silylated allenol ethers.Among the compounds prepared were alkenyl, alkynyl and acyl silyl ketones.The spectroscopic properties of representative members of these classes of comp