Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H12O |
| Molecular Weight | 148.2017 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC=C2CCCCC2=C1
InChI
InChIKey=UMKXSOXZAXIOPJ-UHFFFAOYSA-N
InChI=1S/C10H12O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h5-7,11H,1-4H2
| Molecular Formula | C10H12O |
| Molecular Weight | 148.2017 |
| 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 |
|---|---|---|
| Photodegradation of the steroid hormones 17beta-estradiol (E2) and 17alpha-ethinylestradiol (EE2) in dilute aqueous solution. | 2008-11 |
|
| Removal of estrogenic activity and formation of oxidation products during ozonation of 17alpha-ethinylestradiol. | 2004-10-01 |
|
| Non-radiative depletion of the excited electronic states of 9-cyanoanthracene in presence of tetrahydronaphthols. | 2003-02 |
|
| Estrone 3-sulfate mimics, inhibitors of estrone sulfatase activity: homology model construction and docking studies. | 2002-12-17 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:31:46 GMT 2025
by
admin
on
Mon Mar 31 19:31:46 GMT 2025
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| Record UNII |
TMR02I7N8S
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| Record Status |
Validated (UNII)
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| Record Version |
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1125-78-6
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65604
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C019106
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