4-Cycloocten-1-one

Base Information

• Chemical Name: 4-Cycloocten-1-one
• CAS No.: 297752-29-5
• Molecular Formula: C₈H₁₂O
• Molecular Weight: 124.183
• Nikkaji Number: J607.758G
• Mol file: 297752-29-5.mol

Synonyms:4-Cycloocten-1-one;6925-14-0;4-cyclooctenone;cyclooct-4-en-1-one;SCHEMBL1566775;QCMJRQVMECBHEA-UPHRSURJSA-N;AKOS024436688;AT27795

Chemical Property of 4-Cycloocten-1-one

Chemical Property:

• XLogP3: 1.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 124.088815002
• Heavy Atom Count: 9
• Complexity: 125

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1CC=CCCC(=O)C1
• Isomeric SMILES: C1C/C=C\CCC(=O)C1

Technology Process of 4-Cycloocten-1-one

There total 8 articles about 4-Cycloocten-1-one 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:

1,2-cyclooctene (931-88-4,22770-27-0,3958-30-3,25267-51-0) → Cyclooctene oxide (286-62-4) + cycloactanone (502-49-8) + 1,2-cyclooctanediol (4277-32-1) + cyclooct-4-en-1-one (297752-29-5,297752-30-8) + 2-cycloocten-1-one (1728-25-2)

Guidance literature:

With tert.-butylhydroperoxide; Nd_0.05Ni_0.95Fe₂O₄; In water; acetonitrile; at 85 ℃; for 0.5h; Time; Solvent; Reagent/catalyst; chemoselective reaction; Mechanism;

DOI:10.1007/s13738-020-01983-2

Reference yield:

1,2-cyclooctene (931-88-4,22770-27-0,3958-30-3,25267-51-0) → Cyclooctene oxide (286-62-4) + cycloactanone (502-49-8) + 2-hydroxycylooctanone (496-82-2) + 1,2-cyclooctanediol (4277-32-1) + cyclooct-4-en-1-one (297752-29-5,297752-30-8) + 2-cycloocten-1-one (1728-25-2)

Guidance literature:

With tert.-butylhydroperoxide; Ce_0.05Ni_0.95Fe₂O₄; In water; acetonitrile; at 85 ℃; for 2h; Time; Solvent; Reagent/catalyst; chemoselective reaction; Mechanism;

DOI:10.1007/s13738-020-01983-2

Reference yield:

1,2-cyclooctene (931-88-4,22770-27-0,3958-30-3,25267-51-0) → Cyclooctene oxide (286-62-4) + cycloactanone (502-49-8) + cyclooct-4-en-1-one (297752-29-5,297752-30-8) + 2-cycloocten-1-one (1728-25-2)

Guidance literature:

With tert.-butylhydroperoxide; Ce_0.05Ni_0.95Fe₂O₄; In water; acetonitrile; at 85 ℃; for 2h; Time; Solvent; Reagent/catalyst; chemoselective reaction; Mechanism;

DOI:10.1007/s13738-020-01983-2

upstream raw materials:

cis-Cyclooctene

1,2-cyclooctene

Downstream raw materials:

dibenzyl (2E,10E)-6-oxododeca-2,10-dienedioate