Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H22O |
| Molecular Weight | 182.3025 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1CCCCCCCCCCC1
InChI
InChIKey=SXVPOSFURRDKBO-UHFFFAOYSA-N
InChI=1S/C12H22O/c13-12-10-8-6-4-2-1-3-5-7-9-11-12/h1-11H2
| Molecular Formula | C12H22O |
| Molecular Weight | 182.3025 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Bioproduction of lauryl lactone and 4-vinyl guaiacol as value-added chemicals in two-phase biotransformation systems. | 2009-10 |
|
| Investigation on the Beckmann rearrangement reaction catalyzed by porous solids: MAS NMR and theoretical calculations. | 2009-04 |
|
| Design, synthesis, and fungicidal activity of macrolactones and macrolactams with a sulfonamide side chain. | 2008-08-13 |
|
| Beckmann rearrangement of ketoximes to lactams by triphosphazene catalyst. | 2008-04-04 |
|
| 2-(Methyl-sulfan-yl)cyclo-dodeca-none tosyl-hydrazone. | 2008-03-05 |
|
| Cyanuric chloride as a mild and active Beckmann rearrangement catalyst. | 2005-08-17 |
|
| Sesquiterpenes from the red alga Laurencia tristicha. | 2005-06 |
|
| Synthesis and fungicidal activity of novel 2-oxocycloalkylsulfonylureas. | 2005-03-23 |
|
| The gossypol-cyclododecanone (1/2) inclusion complex. | 2003-07 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:54:37 GMT 2025
by
admin
on
Mon Mar 31 19:54:37 GMT 2025
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| Record UNII |
WL053118A9
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| Record Status |
Validated (UNII)
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| Record Version |
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Cyclododecanone
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