Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H11NO |
| Molecular Weight | 149.1897 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)NC1=CC=CC=C1
InChI
InChIKey=ZTHRQJQJODGZHV-UHFFFAOYSA-N
InChI=1S/C9H11NO/c1-2-9(11)10-8-6-4-3-5-7-8/h3-7H,2H2,1H3,(H,10,11)
| Molecular Formula | C9H11NO |
| Molecular Weight | 149.1897 |
| 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 |
|---|---|---|
| Mefenacet [2-(1,3-benzothia-zol-2-yl-oxy)-N-methyl-N-phenyl-acetamide]. | 2010-11-13 |
|
| Forced degradation of fentanyl: identification and analysis of impurities and degradants. | 2010-11-02 |
|
| Identification of isobaric product ions in electrospray ionization mass spectra of fentanyl using multistage mass spectrometry and deuterium labeling. | 2010-09-15 |
|
| Synthesis and anticonvulsant activity of some alkanamide derivatives. | 2010 |
|
| Potential biomarkers of smoked fentanyl utilizing pyrolysis gas chromatography-mass spectrometry. | 2009-10 |
|
| Pharmacogenetic determinants of human liver microsomal alfentanil metabolism and the role of cytochrome P450 3A5. | 2005-03 |
|
| Metabolism of alfentanil by cytochrome p4503a (cyp3a) enzymes. | 2005-03 |
|
| Long-acting fentanyl analogues: synthesis and pharmacology of N-(1-phenylpyrazolyl)-N-(1-phenylalkyl-4-piperidyl)propanamides. | 2002-03 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:29:29 GMT 2025
by
admin
on
Mon Mar 31 21:29:29 GMT 2025
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| Record UNII |
UYP5ZQI00T
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| Record Status |
Validated (UNII)
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210-649-3
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12107
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620-71-3
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UYP5ZQI00T
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DTXSID0060721
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58952
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| Related Record | Type | Details | ||
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PARENT -> METABOLITE INACTIVE |
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PARENT -> METABOLITE INACTIVE |
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| Related Record | Type | Details | ||
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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