Details
| Stereochemistry | MIXED |
| Molecular Formula | C17H20O |
| Molecular Weight | 240.3401 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1(C)C2CCC1(C)C(=O)\C2=C\C3=CC=CC=C3
InChI
InChIKey=OIQXFRANQVWXJF-ACCUITESSA-N
InChI=1S/C17H20O/c1-16(2)14-9-10-17(16,3)15(18)13(14)11-12-7-5-4-6-8-12/h4-8,11,14H,9-10H2,1-3H3/b13-11+
| Molecular Formula | C17H20O |
| Molecular Weight | 240.3401 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 1 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Estrogenic activity and estrogen receptor beta binding of the UV filter 3-benzylidene camphor. Comparison with 4-methylbenzylidene camphor. | 2004 Jul 1 |
|
| Female sexual behavior, estrous cycle and gene expression in sexually dimorphic brain regions after pre- and postnatal exposure to endocrine active UV filters. | 2009 Mar |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:41:59 GMT 2023
by
admin
on
Fri Dec 15 15:41:59 GMT 2023
|
| Record UNII |
2F60H204CM
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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| Code System | Code | Type | Description | ||
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239-139-9
Created by
admin on Fri Dec 15 15:41:59 GMT 2023 , Edited by admin on Fri Dec 15 15:41:59 GMT 2023
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15087-24-8
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admin on Fri Dec 15 15:41:59 GMT 2023 , Edited by admin on Fri Dec 15 15:41:59 GMT 2023
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DTXSID90864552
Created by
admin on Fri Dec 15 15:41:59 GMT 2023 , Edited by admin on Fri Dec 15 15:41:59 GMT 2023
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2F60H204CM
Created by
admin on Fri Dec 15 15:41:59 GMT 2023 , Edited by admin on Fri Dec 15 15:41:59 GMT 2023
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5901612
Created by
admin on Fri Dec 15 15:41:59 GMT 2023 , Edited by admin on Fri Dec 15 15:41:59 GMT 2023
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C511303
Created by
admin on Fri Dec 15 15:41:59 GMT 2023 , Edited by admin on Fri Dec 15 15:41:59 GMT 2023
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