Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H10O |
| Molecular Weight | 170.2072 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)C1=C2C=CC=CC2=CC=C1
InChI
InChIKey=QQLIGMASAVJVON-UHFFFAOYSA-N
InChI=1S/C12H10O/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11/h2-8H,1H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| A ruthenium-catalyzed reaction of aromatic ketones with arylboronates: a new method for the arylation of aromatic compounds via C-H bond cleavage. | 2003 Feb 19 |
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| Improvement of carbonyl reductase production of Geotrichum candidum for the transformation of 1-acetonaphthone to S(-)-1-(1'-napthyl) ethanol. | 2007 Jul |
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| Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism. | 2008 Apr |
|
| Toxicity, tunneling and feeding behavior of the termite, Coptotermes vastator, in sand treated with oil of the physic nut, Jatropha curcas. | 2009 |
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| Synthesis and antihyperglycemic activity of 2-(substituted phenyl)-3-{[4-(1-naphthyl)-1,3-thiazol-2-yl] amino}-4-oxo-1,3-thiazolidin-5-ylacetic acid derivatives. | 2009 Jan-Feb |
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| (E)-3-(4-Chloro-phen-yl)-1-(1-naphth-yl)prop-2-en-1-one. | 2009 Nov 28 |
|
| (2E)-3-(2-Chloro-6-methyl-3-quinol-yl)-1-(1-naphth-yl)prop-2-en-1-one. | 2010 Mar 6 |
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941-98-0
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DTXSID4052635
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213-384-1
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7659
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13663
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U44R403XVS
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SUBSTANCE RECORD
