Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C7H12O |
| Molecular Weight | 112.1696 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O[C@H]1C[C@@H]2CC[C@H]1C2
InChI
InChIKey=ZQTYQMYDIHMKQB-VQVTYTSYSA-N
InChI=1S/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7+/m1/s1
| Molecular Formula | C7H12O |
| Molecular Weight | 112.1696 |
| 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 |
|---|---|---|
| Comparative analysis of chemical compositions and antimicrobial activities of essential oils from Abies holophylla and Abies koreana activities of essential oils from Abies holophylla and Abies koreana. | 2009-04 |
|
| Interpretation of conformational effects on 2-endo-norborneol by natural chemical shielding analysis. | 2005-02-10 |
|
| Inversion vs retention of configuration in gas-phase ammonium ion/alcohol reactions. | 2002-02-22 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 17:02:10 GMT 2025
by
admin
on
Tue Apr 01 17:02:10 GMT 2025
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| Record UNII |
AF39IU2W1C
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| Record Status |
Validated (UNII)
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11040657
Created by
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AF39IU2W1C
Created by
admin on Tue Apr 01 17:02:10 GMT 2025 , Edited by admin on Tue Apr 01 17:02:10 GMT 2025
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61277-93-8
Created by
admin on Tue Apr 01 17:02:10 GMT 2025 , Edited by admin on Tue Apr 01 17:02:10 GMT 2025
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| Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER |