Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H13NO2 |
| Molecular Weight | 167.205 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(O)C=C(CCN)C=C1
InChI
InChIKey=WJXQFVMTIGJBFX-UHFFFAOYSA-N
InChI=1S/C9H13NO2/c1-12-9-3-2-7(4-5-10)6-8(9)11/h2-3,6,11H,4-5,10H2,1H3
| Molecular Formula | C9H13NO2 |
| Molecular Weight | 167.205 |
| 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 |
|---|---|---|
| Calcium-promoted Pictet-Spengler reactions of ketones and aldehydes. | 2010-12-17 |
|
| Human and mouse trace amine-associated receptor 1 have distinct pharmacology towards endogenous monoamines and imidazoline receptor ligands. | 2009-10-23 |
|
| Effect of methyl derivatives of dopamine on tumor necrosis factor alpha and lipid peroxidation. | 2007-12 |
|
| N-caffeoylphenalkylamide derivatives as bacterial efflux pump inhibitors. | 2007-03-15 |
|
| Cinnamic acid amides from Chenopodium album: effects on seeds germination and plant growth. | 2003-12 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:01:51 GMT 2025
by
admin
on
Mon Mar 31 19:01:51 GMT 2025
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| Record UNII |
62MI76A89G
|
| Record Status |
Validated (UNII)
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| Record Version |
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1225215
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