Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H14O2 |
| Molecular Weight | 166.217 |
| Optical Activity | ( - ) |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H]1CC[C@@H]([C@@H]1C=O)C(=C)C=O
InChI
InChIKey=BORBLDJNKYHVJP-FXBDTBDDSA-N
InChI=1S/C10H14O2/c1-7-3-4-9(8(2)5-11)10(7)6-12/h5-7,9-10H,2-4H2,1H3/t7-,9+,10+/m0/s1
| Molecular Formula | C10H14O2 |
| Molecular Weight | 166.217 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| A divergent approach to the diastereoselective synthesis of several ant-associated iridoids. | 2010-04-02 |
|
| Relative configuration of natural products using NMR chemical shifts. | 2009-04 |
|
| Dolichodial: a new aphid sex pheromone component? | 2008-12 |
|
| An unexpected mixture of substances in the defensive secretions of the tubuliferan thrips, Callococcithrips fuscipennis (Moulton). | 2008-06 |
|
| Developmental and geographical variation in the chemical defense of the walkingstick insect Anisomorpha buprestoides. | 2008-05 |
|
| Single insect NMR: A new tool to probe chemical biodiversity. | 2006-09-19 |
|
| Chemical composition, antimicrobial and antioxidant activity of the essential oil of Teucrium marum (Lamiaceae). | 2005-04-08 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:48:46 GMT 2025
by
admin
on
Mon Mar 31 22:48:46 GMT 2025
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| Record UNII |
1KLH0PK5RS
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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60478-52-6
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m4729
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1KLH0PK5RS
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442422
Created by
admin on Mon Mar 31 22:48:46 GMT 2025 , Edited by admin on Mon Mar 31 22:48:46 GMT 2025
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| Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER |
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ENANTIOMER -> ENANTIOMER |
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