Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H15NO |
| Molecular Weight | 165.2322 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(CC(C)N)=CC=C1
InChI
InChIKey=VEJWNIYARKAHFI-UHFFFAOYSA-N
InChI=1S/C10H15NO/c1-8(11)6-9-4-3-5-10(7-9)12-2/h3-5,7-8H,6,11H2,1-2H3
| Molecular Formula | C10H15NO |
| Molecular Weight | 165.2322 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Biotransformation of 2-, 3-, and 4-methoxy-amphetamines by Cunninghamella echinulata. | 1991-10 |
|
| The metabolism of 3-methoxyamphetamine in dog, monkey and man. | 1981-02 |
|
| Effects of d-amphetamine, monomethoxyamphetamines and hallucinogens on schedule-controlled behavior. | 1978-01 |
|
| Comparative actions of monomethoxyamphetamines on the release and uptake of biogenic amines in brain tissue. | 1976-05 |
|
| Pharmacological evidence for the central serotonergic effects of monomethoxyamphetamines. | 1976-05 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 16:22:09 GMT 2025
by
admin
on
Tue Apr 01 16:22:09 GMT 2025
|
| Record UNII |
C2B7C98LY8
|
| Record Status |
Validated (UNII)
|
| Record Version |
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-
Download
| Name | Type | Language | ||
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Preferred Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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17862-85-0
Created by
admin on Tue Apr 01 16:22:09 GMT 2025 , Edited by admin on Tue Apr 01 16:22:09 GMT 2025
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PRIMARY | |||
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3-Methoxyamphetamine
Created by
admin on Tue Apr 01 16:22:09 GMT 2025 , Edited by admin on Tue Apr 01 16:22:09 GMT 2025
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C2B7C98LY8
Created by
admin on Tue Apr 01 16:22:09 GMT 2025 , Edited by admin on Tue Apr 01 16:22:09 GMT 2025
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152234
Created by
admin on Tue Apr 01 16:22:09 GMT 2025 , Edited by admin on Tue Apr 01 16:22:09 GMT 2025
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DTXSID00939104
Created by
admin on Tue Apr 01 16:22:09 GMT 2025 , Edited by admin on Tue Apr 01 16:22:09 GMT 2025
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PRIMARY |
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|---|---|---|---|---|
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