Ethyl propenyl ether

Base Information

• Chemical Name: Ethyl propenyl ether
• CAS No.: 4696-26-8
• Molecular Formula: C5H10O
• Molecular Weight: 86.1338
• European Community (EC) Number: 213-176-0
• UNII: JH817DUE12
• Nikkaji Number: J27.120I,J340.834E
• Mol file: 4696-26-8.mol

Synonyms:Ethyl propenyl ether;928-55-2;(E)-1-ethoxyprop-1-ene;1-Ethoxypropene;Propenyl ethyl ether;Ether, ethyl propenyl;4696-26-8;trans-1-Ethoxypropene;1-ETHOXY-1-PROPENE;1-Propene, 1-ethoxy-, (E)-;(E)-1-Ethoxypropene;(E)-1-Propenyl ethyl ether;trans-Ethyl propenyl ether;trans-Propenyl ethyl ether;Ethyl trans-1-propenyl ether;Ether, ethyl propenyl, (E)-;1-Propenyl ethyl ether, (E)-;UNII-JH817DUE12;JH817DUE12;Ethyl 1-propenyl ether;1-Propene, 1-ethoxy-;Ethyl-1-propenyl ether;1-Propene, 1-ethoxy-, (1E)-;NSC 6107;EINECS 213-176-0;UNII-4TK5QAZ92W;(E)-1-ethoxy-1-propene;BRN 1735974;MFCD00015184;(1E)-1-ethoxyprop-1-ene;3-01-00-01871 (Beilstein Handbook Reference);1-Etoxipropeno;ETHYLPropenyl ether;1-etoxi-1-propeno,;1-Propeno, 1-etoxi-;C2H5OCH=CHCH3;ethyl (1-propenyl) ether;Ethyl propenyl ether, cis + trans;Ether ethyl propenyl (6CI7CI8CI);trans-1-ethoxy-propene;trans-CH3CH=CH-OC2H5;4TK5QAZ92W;Ethyl 1-propenyl ether, cis + trans;AKOS000121869;LS-67842;EN300-29202;A844368;Q27281505;F8886-8258;Z281777810

Chemical Property of Ethyl propenyl ether

Chemical Property:

• XLogP3: 1.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 86.073164938
• Heavy Atom Count: 6
• Complexity: 39.2

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC=CC
• Isomeric SMILES: CCO/C=C/C

Technology Process of Ethyl propenyl ether

There total 1 articles about Ethyl propenyl ether which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

3-ethoxyprop-1-ene (557-31-3) → (Z)-1-ethoxyprop-1-ene (4696-25-7) + (E)-1-ethoxyprop-1-ene (4696-26-8) + ethylpropylether (628-32-0)

Guidance literature:

With hydrogen; aluminum oxide; nickel; at -0.1 ℃; for 1h; Product distribution; oth. catalyst, time dependence;

DOI:10.1246/bcsj.57.3323

Reference yield: 92.0%

(E)-1-ethoxyprop-1-ene (4696-26-8) + 2-Methyl-2-(phenylseleno)malononitrile (141439-28-3) → 2-(2-Ethoxy-1-methyl-2-phenylselanyl-ethyl)-2-methyl-malononitrile (141439-41-0,141439-42-1)

Guidance literature:

With 2,2'-azobis(isobutyronitrile); In chloroform; at 60 ℃; for 70h;

DOI:10.1021/ja00037a080

Reference yield: 87.0%

(E)-1-ethoxyprop-1-ene (4696-26-8) + (2R,4aR,6S,8aR)-7-Eth-(E)-ylidene-6-methoxy-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-8-one (114047-67-5) → (3R,4aR,6S,7S,8S,9S,10aR)-6-Ethoxy-9-methoxy-7,8-dimethyl-3-phenyl-1,4a,7,8,9,10a-hexahydro-6H-2,4,5,10-tetraoxa-phenanthrene

Guidance literature:

tris(6,6,7,7,8,8-heptafluoro-2,2-dimethyl-3,5-octadionato)europium(III); In hexane; Heating;

DOI:10.1039/c39870000884

upstream raw materials:

3-ethoxyprop-1-ene

Downstream raw materials:

(3R,4R)-3-Ethoxy-4-methyl-2,2-diphenyl-cyclobutanone

(6R,7R,8S)-6-Ethoxy-8-(4-methoxy-phenyl)-7-methyl-7,8-dihydro-6H-[1,3]dioxolo[4,5-g]chromene

(2R,3R,4S)-2-Ethoxy-3-methyl-4-phenyl-chroman

(2S,3S,4S)-2-Ethoxy-3-methyl-4-phenyl-chroman

Refernces