Dihydro-5-(2-octenyl)-2(3H)-furanone

Base Information

Chemical Name:Dihydro-5-(2-octenyl)-2(3H)-furanone
CAS No.:15456-69-6
Molecular Formula:C₁₂H₂₀O₂
Molecular Weight:196.29
Hs Code.:
Nikkaji Number:J475.292I,J2.945.240G
Metabolomics Workbench ID:44608
Mol file:15456-69-6.mol

Synonyms:5-[(E)-oct-2-enyl]oxolan-2-one;Dihydro-5-(2-octenyl)-2(3H)-furanone;(Z)-6-dodecen-gamma-lactone,dihydro-5-(2-octenyl)-2(3H)-furanone,4-hydroxy-gamma-lactone-6-dodecenoicacid;(Z)-6-dodeceno-.gamma.-lactone;6-Dodecen-4-olide;6-dodeceno-.gamma.-lactone;6-Dodecenyl-.gamma.-lactone;SCHEMBL2597399;CHEBI:172045;QFXOXDSHNXAFEY-VOTSOKGWSA-N;5-(2-Octenyl)tetrahydrofuran-2-one;6-Dodeceno-laquo gammaRaquo -lactone;6-Dodecenyl-laquo gammaRaquo -lactone;2(3H)-Furanone, dihydro-5-(2-octenyl);4-Hydroxy-6-dodecenoic acid gamma-lactone;5-[(2E)-oct-2-en-1-yl]oxolan-2-one;5-[(E)-2-Octenyl]tetrahydrofuran-2-one

Suppliers and Price of Dihydro-5-(2-octenyl)-2(3H)-furanone

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of Dihydro-5-(2-octenyl)-2(3H)-furanone

Chemical Property:

PSA：26.30000
LogP:3.21860
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:196.146329876
Heavy Atom Count:14
Complexity:197

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCC=CCC1CCC(=O)O1
Isomeric SMILES:CCCCC/C=C/CC1CCC(=O)O1

Technology Process of Dihydro-5-(2-octenyl)-2(3H)-furanone

There total 5 articles about Dihydro-5-(2-octenyl)-2(3H)-furanone 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: 88.0%

: 73697-60-6
ethyl 3-(oxiran-2-yl)propanoate

: 15456-69-6,60551-23-7,63357-98-2,63357-99-3,127127-84-8,18679-18-0
2(3H)-furanone, dihydro-5-(2-octenyl)-, (Z)-

Guidance literature:: In diethyl ether; 1.) -30 deg C --> -10 deg C, 1 h 2.) -10 deg C, 1h;
DOI:10.1016/0040-4020(80)80209-2

Reference yield:

: 1968-40-7
ethyl 4-pentenoate

: 15456-69-6,60551-23-7,63357-98-2,63357-99-3,127127-84-8,18679-18-0
2(3H)-furanone, dihydro-5-(2-octenyl)-, (Z)-

Guidance literature:: Multi-step reaction with 2 steps

1: 87 percent / MCPBA / CH₂Cl₂

2: 88 percent / diethyl ether / 1.) -30 deg C --> -10 deg C, 1 h 2.) -10 deg C, 1h

With 3-chloro-benzenecarboperoxoic acid; In diethyl ether; dichloromethane;
DOI:10.1016/0040-4020(80)80209-2

Reference yield:

: 4762-26-9
hexyltriphenylphosphonium bromide

: 134359-16-3
γ-(prop-2-enyl)-γ-butyrolactone

: 15456-69-6,60551-23-7,63357-98-2,63357-99-3,127127-84-8,18679-18-0
2(3H)-furanone, dihydro-5-(2-octenyl)-, (Z)-

Guidance literature:: With n-butyllithium; hydrogen; ozone; palladium on activated charcoal; Yield given. Multistep reaction; 1.) EtOAc, -70 deg C; 2.) EtOAc, -10 deg C, then Rt; 3.) hexane, toluene, -70 deg C to Rt, 1 h;
DOI:10.1002/hlca.19820650204