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
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Oxidation of hydroquinone, 2,3-dimethylhydroquinone and 2,3,5-trimethylhydroquinone by human myeloperoxidase. | 2000 |
|
| Studies of all-trans-retinal as a photooxidizing agent. | 2001 Jan |
|
| Anti-HSV-1 activity of synthetic humic acid-like polymers derived from p-diphenolic starting compounds. | 2002 Jul |
|
| Electrochemical oxidation of 2,3-dimethylhydroquinone in the presence of 1,3-dicarbonyl compounds. | 2006 Mar 3 |
|
| Enantioselective total synthesis of the natural gamma-tocopherol metabolite (S)-gamma-CEHC [(S)-LLU-alpha]. | 2010 Feb 5 |
|
| 1,7-Dimethyl-penta-cyclo-[5.4.0.0.0.0]undecane-8,11-dione. | 2010 Jul 3 |
Patents
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| Code System | Code | Type | Description | ||
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108080
Created by
admin on Fri Dec 15 19:29:38 GMT 2023 , Edited by admin on Fri Dec 15 19:29:38 GMT 2023
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608-43-5
Created by
admin on Fri Dec 15 19:29:38 GMT 2023 , Edited by admin on Fri Dec 15 19:29:38 GMT 2023
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DTXSID50870679
Created by
admin on Fri Dec 15 19:29:38 GMT 2023 , Edited by admin on Fri Dec 15 19:29:38 GMT 2023
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F0L7HG609J
Created by
admin on Fri Dec 15 19:29:38 GMT 2023 , Edited by admin on Fri Dec 15 19:29:38 GMT 2023
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69100
Created by
admin on Fri Dec 15 19:29:38 GMT 2023 , Edited by admin on Fri Dec 15 19:29:38 GMT 2023
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SUBSTANCE RECORD
