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 |
---|---|---|
Estrone 3-sulfate mimics, inhibitors of estrone sulfatase activity: homology model construction and docking studies. | 2002 Dec 17 |
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Non-radiative depletion of the excited electronic states of 9-cyanoanthracene in presence of tetrahydronaphthols. | 2003 Feb |
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Removal of estrogenic activity and formation of oxidation products during ozonation of 17alpha-ethinylestradiol. | 2004 Oct 1 |
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Photodegradation of the steroid hormones 17beta-estradiol (E2) and 17alpha-ethinylestradiol (EE2) in dilute aqueous solution. | 2008 Nov |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:04:59 GMT 2023
by
admin
on
Fri Dec 15 19:04:59 GMT 2023
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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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-
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1125-78-6
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65604
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214-410-4
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C019106
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TMR02I7N8S
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14305
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