Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H10O2 |
| Molecular Weight | 138.1638 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(O)C=CC(O)=C1C
InChI
InChIKey=BXJGUBZTZWCMEX-UHFFFAOYSA-N
InChI=1S/C8H10O2/c1-5-6(2)8(10)4-3-7(5)9/h3-4,9-10H,1-2H3
| Molecular Formula | C8H10O2 |
| Molecular Weight | 138.1638 |
| 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 |
|---|---|---|
| 1,7-Dimethyl-penta-cyclo-[5.4.0.0.0.0]undecane-8,11-dione. | 2010-07-03 |
|
| Enantioselective total synthesis of the natural gamma-tocopherol metabolite (S)-gamma-CEHC [(S)-LLU-alpha]. | 2010-02-05 |
|
| Electrochemical oxidation of 2,3-dimethylhydroquinone in the presence of 1,3-dicarbonyl compounds. | 2006-03-03 |
|
| Anti-HSV-1 activity of synthetic humic acid-like polymers derived from p-diphenolic starting compounds. | 2002-07 |
|
| An N,N'-dialkyl-4,4'-bipyridinium-modified titanium-dioxide photocatalyst for water remediation--observation and application of supramolecular effects in photocatalytic degradation of pi-donor organic compounds. | 2001-11 |
|
| Studies of all-trans-retinal as a photooxidizing agent. | 2001-01 |
|
| Oxidation of hydroquinone, 2,3-dimethylhydroquinone and 2,3,5-trimethylhydroquinone by human myeloperoxidase. | 2000 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:45:51 GMT 2025
by
admin
on
Mon Mar 31 19:45:51 GMT 2025
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| Record UNII |
F0L7HG609J
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| Record Status |
Validated (UNII)
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| Record Version |
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108080
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608-43-5
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DTXSID50870679
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F0L7HG609J
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69100
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