Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H11NO2 |
| Molecular Weight | 165.1891 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(NC(C)=O)C=C1
InChI
InChIKey=XVAIDCNLVLTVFM-UHFFFAOYSA-N
InChI=1S/C9H11NO2/c1-7(11)10-8-3-5-9(12-2)6-4-8/h3-6H,1-2H3,(H,10,11)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Tris(4-acetamido-phenoxy-methyl)methanol 0.7-hydrate. | 2008-10-25 |
|
| Synthesis and anti-breast cancer activities of substituted quinolines. | 2008-06-01 |
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| Oxidations of p-alkoxyacylanilides catalyzed by human cytochrome P450 1A2: structure-activity relationships and simulation of rate constants of individual steps in catalysis. | 2001-04-10 |
Patents
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51-66-1
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DTXSID6026325
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5827
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C035495
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13E468TFHP
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139354
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100000177449
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m1320
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200-114-2
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SUBSTANCE RECORD
