Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H9NO2 |
| Molecular Weight | 151.1626 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C=C1)C(N)=O
InChI
InChIKey=GUCPYIYFQVTFSI-UHFFFAOYSA-N
InChI=1S/C8H9NO2/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3,(H2,9,10)
| Molecular Formula | C8H9NO2 |
| Molecular Weight | 151.1626 |
| 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 |
|---|---|---|
| 4-Chloro-N-(2-methoxy-phen-yl)benzamide. | 2009-12-19 |
|
| Tandem multi-step synthesis of C-carboxyazlactones promoted by N-heterocyclic carbenes. | 2008-08-14 |
|
| Determination of metabolic stability of positron emission tomography tracers by LC-MS/MS: an example in WAY-100635 and two analogues. | 2006-03-03 |
|
| Naravelia zeylanica [corrected] occurrence of primary benzamides in flowering plants. | 2005-04 |
|
| The aniracetam metabolite 2-pyrrolidinone induces a long-term enhancement in AMPA receptor responses via a CaMKII pathway. | 2002-01-31 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:22:58 GMT 2025
by
admin
on
Mon Mar 31 19:22:58 GMT 2025
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| Record UNII |
Z85FX3977E
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| Record Status |
Validated (UNII)
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| Record Version |
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