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 |
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The gossypol-cyclododecanone (1/2) inclusion complex. | 2003 Jul |
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Cyanuric chloride as a mild and active Beckmann rearrangement catalyst. | 2005 Aug 17 |
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Sesquiterpenes from the red alga Laurencia tristicha. | 2005 Jun |
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Synthesis and fungicidal activity of novel 2-oxocycloalkylsulfonylureas. | 2005 Mar 23 |
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Beckmann rearrangement of ketoximes to lactams by triphosphazene catalyst. | 2008 Apr 4 |
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Design, synthesis, and fungicidal activity of macrolactones and macrolactams with a sulfonamide side chain. | 2008 Aug 13 |
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2-(Methyl-sulfan-yl)cyclo-dodeca-none tosyl-hydrazone. | 2008 Mar 5 |
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Investigation on the Beckmann rearrangement reaction catalyzed by porous solids: MAS NMR and theoretical calculations. | 2009 Apr |
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Bioproduction of lauryl lactone and 4-vinyl guaiacol as value-added chemicals in two-phase biotransformation systems. | 2009 Oct |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:42:58 GMT 2023
by
admin
on
Fri Dec 15 19:42:58 GMT 2023
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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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830-13-7
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Cyclododecanone
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212-595-6
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WL053118A9
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DTXSID3027322
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77116
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