Details
Stereochemistry | ACHIRAL |
Molecular Formula | C9H10O3 |
Molecular Weight | 166.1739 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(CC(O)=O)=CC=C1
InChI
InChIKey=LEGPZHPSIPPYIO-UHFFFAOYSA-N
InChI=1S/C9H10O3/c1-12-8-4-2-3-7(5-8)6-9(10)11/h2-5H,6H2,1H3,(H,10,11)
Approval Year
PubMed
Title | Date | PubMed |
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Contribution of aldehyde oxidase, xanthine oxidase, and aldehyde dehydrogenase on the oxidation of aromatic aldehydes. | 2004 Oct |
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Role of the peri-effect in synthesis and reactivity of highly substituted naphthaldehydes: a novel backbone amide linker for solid-phase synthesis. | 2005 Feb 7 |
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Pilocarpine-induced status epilepticus: monoamine level, muscarinic and dopaminergic receptors alterations in striatum of young rats. | 2005 Jul 22-29 |
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Study of the cytotoxic activity of di and triphenyltin(IV) carboxylate complexes. | 2008 Dec |
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Lipophilic (hydroxy)phenylacetates by solvent-free lipase-catalyzed esterification and transesterification in vacuo. | 2008 Jul 9 |
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Anticancer activity of dinuclear gallium(III) carboxylate complexes. | 2010 Feb |
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DTXSID70170865
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15719
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1798-09-0
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25XLO0T6MY
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217-282-8
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admin on Fri Dec 15 18:38:12 GMT 2023 , Edited by admin on Fri Dec 15 18:38:12 GMT 2023
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SUBSTANCE RECORD