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
CCC1=CC(O)=C(O)C=C1
InChI
InChIKey=HFLGBNBLMBSXEM-UHFFFAOYSA-N
InChI=1S/C8H10O2/c1-2-6-3-4-7(9)8(10)5-6/h3-5,9-10H,2H2,1H3
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 |
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Metabolic activation of carcinogenic ethylbenzene leads to oxidative DNA damage. | 2004 Dec 7 |
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Development of a stable isotope dilution analysis with liquid chromatography-tandem mass spectrometry detection for the quantitative analysis of di- and trihydroxybenzenes in foods and model systems. | 2006 Aug 9 |
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Quantitative precursor studies on di- and trihydroxybenzene formation during coffee roasting using "in bean" model experiments and stable isotope dilution analysis. | 2006 Dec 27 |
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Synthesis and structure determination of covalent conjugates formed from the sulfury-roasty-smelling 2-furfurylthiol and di- or trihydroxybenzenes and their identification in coffee brew. | 2006 Dec 27 |
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Quantitative studies on the formation of phenol/2-furfurylthiol conjugates in coffee beverages toward the understanding of the molecular mechanisms of coffee aroma staling. | 2007 May 16 |
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Determination of 4-ethylcatechol in wine by high-performance liquid chromatography-coulometric electrochemical array detection. | 2008 Feb 25 |
|
Anti-influenza activity of phenethylphenylphthalimide analogs derived from thalidomide. | 2010 Jul 15 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:57:31 GMT 2023
by
admin
on
Fri Dec 15 17:57:31 GMT 2023
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Record UNII |
574JV8BYR2
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Record Status |
Validated (UNII)
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Record Version |
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574JV8BYR2
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214-397-5
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DTXSID50150029
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70761
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