Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H10O2 |
| Molecular Weight | 186.2066 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC=C(OC2=CC=CC=C2)C=C1
InChI
InChIKey=ZSBDGXGICLIJGD-UHFFFAOYSA-N
InChI=1S/C12H10O2/c13-10-6-8-12(9-7-10)14-11-4-2-1-3-5-11/h1-9,13H
| Molecular Formula | C12H10O2 |
| Molecular Weight | 186.2066 |
| 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 |
|---|---|---|
| Variable products in dielectric-barrier discharge assisted benzene oxidation. | 2010-06-15 |
|
| Modulating the substrate specificity of LTA4H aminopeptidase by using chemical compounds and small-molecule-guided mutagenesis. | 2010-05-17 |
|
| Molecular determinants of juvenile hormone action as revealed by 3D QSAR analysis in Drosophila. | 2009-06-23 |
|
| Solar driven production of toxic halogenated and nitroaromatic compounds in natural seawater. | 2008-07-15 |
|
| Different reaction mechanisms of diphenylether and 4-bromodiphenylether with nitrous acid in the 355 nm laser flash photolysis of mixed aqueous solution. | 2008-04 |
|
| Antifouling activity of sponge-derived polybrominated diphenyl ethers and synthetic analogues. | 2008 |
|
| The presumptive detection of benzene in water in the presence of phenol with an active membrane-UV photo-ionisation differential mobility spectrometer. | 2006-09 |
|
| Mechanism of action of sensors for reactive oxygen species based on fluorescein-phenol coupling: the case of 2-[6-(4'-hydroxy)phenoxy-3H-xanthen-3-on-9-yl]benzoic acid. | 2006-03-07 |
|
| Indirect detection of substituted phenols and cannabis based on the electrochemical adaptation of the Gibbs reaction. | 2005-10 |
|
| Atmospheric pressure photoionization mechanisms. 2. The case of benzene and toluene. | 2003 |
|
| In vitro free radical scavenging capacity of thyroid hormones and structural analogues. | 2001-07 |
|
| Design and synthesis of aryloxyethyl thiocyanate derivatives as potent inhibitors of Trypanosoma cruzi proliferation. | 2000-05-04 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:54:23 GMT 2025
by
admin
on
Mon Mar 31 18:54:23 GMT 2025
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| Record UNII |
D83R742GJR
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| Record Status |
Validated (UNII)
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| Record Version |
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25027
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39264
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212-611-1
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