Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H12O |
| Molecular Weight | 124.1803 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)C1=CCCCC1
InChI
InChIKey=LTYLUDGDHUEBGX-UHFFFAOYSA-N
InChI=1S/C8H12O/c1-7(9)8-5-3-2-4-6-8/h5H,2-4,6H2,1H3
| Molecular Formula | C8H12O |
| Molecular Weight | 124.1803 |
| 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 |
|---|---|---|
| The first total synthesis of (-)-solanapyrone E based on domino Michael strategy. | 2001 Jan 25 |
|
| First total syntheses of the phytotoxins solanapyrones D and E via the domino Michael protocol. | 2002 Aug 23 |
|
| Stereoselective three-component synthesis of trans-endo-decahydroquinolin-4-one derivatives from aldehydes, aniline, and acetylcyclohexene. | 2006 Aug 18 |
|
| High-throughput kinetic study of hydrogenation over palladium nanoparticles: combination of reaction and analysis. | 2008 |
|
| Direct asymmetric catalytic thienylaluminum addition to ketones: a concise approach to the synthesis of (S)-tiemonium iodide. | 2009 Aug 6 |
|
| Allylic oxidations catalyzed by dirhodium caprolactamate via aqueous tert-butyl hydroperoxide: the role of the tert-butylperoxy radical. | 2009 Jan 16 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:32:57 GMT 2023
by
admin
on
Fri Dec 15 19:32:57 GMT 2023
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| Record UNII |
7539U6WQBL
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| Record Status |
Validated (UNII)
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| Record Version |
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