4696-25-7

Basic information

• Product Name: (Z)-1-ethoxyprop-1-ene
• CAS NO: 4696-25-7
• Molecular Formula: C₅H₁₀O
• Molecular Weight: 86.1338
• Mol File: 4696-25-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 68.2°Cat760mmHg
• Flash Point: °C
• Density: 0.775g/cm³
• CAS DataBase Reference: (Z)-1-ethoxyprop-1-ene(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-1-ethoxyprop-1-ene(4696-25-7)
• EPA Substance Registry System: (Z)-1-ethoxyprop-1-ene(4696-25-7)

Safety Data

• Hazardous Substances Data: 4696-25-7(Hazardous Substances Data)

Usage

Description

(Z)-1-ethoxyprop-1-ene, also known as ethyl vinyl ether, is a colorless, flammable liquid with a sweet, ether-like odor. It is a chemical compound with the molecular formula C5H10O. (Z)-1-ethoxyprop-1-ene is known for its versatile applications in various industries due to its unique properties.

Uses

Used in Solvent Applications:
(Z)-1-ethoxyprop-1-ene is used as a solvent for various organic compounds due to its ability to dissolve a wide range of substances. Its solvent properties make it a valuable component in the chemical industry.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, (Z)-1-ethoxyprop-1-ene is used as an intermediate in the synthesis of various organic compounds. Its role in the production of pharmaceuticals highlights its importance in the development of new drugs and medications.
Used in Polymer Production:
(Z)-1-ethoxyprop-1-ene also serves as a monomer in the production of polymers. Its ability to form polymers contributes to its use in the plastics and materials science industries, where it can be utilized to create a variety of products with specific properties.
Used in Chemical Synthesis:
(Z)-1-ethoxyprop-1-ene is used as an intermediate in the synthesis of various organic compounds, making it a crucial component in the development of new chemicals and materials.
Safety Precautions:

Upstream product

• 4696-26-8 (E)-1-ethoxyprop-1-ene 
• 557-31-3 3-ethoxyprop-1-ene 

Downstream Products

• 32929-60-5 3-ethoxy-4-methyl-2,2-diphenylcyclobutanone 
• 49748-20-1 2-(2-Formylpropyl)-3-isopropenyl-1-methyl-cyclopent-1-en 
• 49748-25-6 3-isopropenyl-1-methyl-2-methylene-cyclopentan-1-ol 
• 10602-37-6 1,1,3,3-tetraethoxy-2-methyl-propane 
• 68519-95-9 1,2-Di-<(1'-ethoxy)-propoxy>-propan 
• 102103-14-0 (2S,3S,4R)-4-Benzyl-2-ethoxy-3-methyl-chroman 
• 102102-95-4 (2S,3S,4S)-2-Ethoxy-3-methyl-4-phenyl-chroman 
• 115096-22-5 (2R,3S,4R)-4-Benzyloxy-6-benzyloxymethyl-2-ethoxy-3-methyl-5-phenylsulfanyl-3,4-dihydro-2H-pyran 
• 115096-25-8 Ethyl-4-O-acetyl-3,6-di-O-benzyl-2-desoxy-2-methyl-β-DL-mannopyranosid 
• 115096-36-1 Ethyl-3,6-di-O-benzyl-2-desoxy-2-methyl-β-DL-lyxo-4-hexulopyranosid 
• 115182-40-6 (2α,3α,4α)-6-(Benzyloxymethyl)-2-ethoxy-3,4-dihydro-4-hydroxy-3-methyl-5-phenylthio-2H-pyran 
• 115096-37-2 Ethyl-3,6-di-O-benzyl-2,4-didesoxy-2-methyl-4-methylen-β-DL-lyxo-hexopyranosid 
• 115096-23-6 (2S,3R,4R)-4-Benzyloxy-6-benzyloxymethyl-2-ethoxy-3-methyl-3,4-dihydro-2H-pyran 
• 115096-24-7 Ethyl-3,6-di-O-benzyl-2-desoxy-2-methyl-β-DL-mannopyranosid 

Relevant articles and documents

Isomerization of allylic alcohols to carbonyl compounds by aqueous-biphase rhodium catalysis

Isomerization of allylic and homoallylic alcohols is catalyzed by the zwitterionic Rh(I) complex (sulphos)Rh(cod) in water-n-octane to give the corresponding aldehyde or ketone in high yields and chemoselectivity. A π-allyl metal hydride mechanism is proposed on the basis of various independent experiments in both homogeneous and biphasic systems [sulphos = -O3S(C6H4)CH2C(CH2 PPh2)3].