Details
Stereochemistry | ACHIRAL |
Molecular Formula | C9H10O |
Molecular Weight | 134.1751 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC=CC=C1CC=C
InChI
InChIKey=QIRNGVVZBINFMX-UHFFFAOYSA-N
InChI=1S/C9H10O/c1-2-5-8-6-3-4-7-9(8)10/h2-4,6-7,10H,1,5H2
Molecular Formula | C9H10O |
Molecular Weight | 134.1751 |
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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Inhibition of rat, mouse, and human glutathione S-transferase by eugenol and its oxidation products. | 1996 Jan 5 |
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Novel generation of an o-quinone methide from 2-(2'-cyclohexenyl)phenol by excited state intramolecular proton transfer and subsequent C-C fragmentation. | 2002 Nov 21 |
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Picoamperometric detection of glucose at ultrasmall platinum-based biosensors: preparation and characterization. | 2003 Jul 15 |
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Deuterium-labeling studies establishing stereochemistry at the oxypalladation step in Wacker-type oxidative cyclization of an o-allylphenol. | 2004 Mar 17 |
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Male sex pheromonal components derived from methyl eugenol in the hemolymph of the fruit fly Bactrocera papayae. | 2004 Nov |
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Reaction of benzoxasilocines with aromatic aldehydes: Synthesis of homopterocarpans. | 2007 Feb 8 |
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Mechanistic insights into the palladiumII-catalyzed hydroxyalkoxylation of 2-allylphenols. | 2007 Mar 2 |
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Chloroperoxidase, a janus enzyme. | 2008 Mar 4 |
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Inhibitory effect of bionic fungicide 2-allylphenol on Botrytis cinerea (Pers. ex Fr.) in vitro. | 2009 Dec |
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Isolation of an unusual metabolite 2-allyloxyphenol from a marine actinobacterium, its biological activities and applications. | 2010 Mar |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:47:30 GMT 2023
by
admin
on
Fri Dec 15 17:47:30 GMT 2023
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Record UNII |
O04F145ZJZ
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Record Status |
Validated (UNII)
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Record Version |
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