Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C11H15NO3 |
| Molecular Weight | 209.2417 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC2=C(OCO2)C=C1CC(C)N
InChI
InChIKey=GPVJAXJRAZVITB-UHFFFAOYSA-N
InChI=1S/C11H15NO3/c1-7(12)3-8-4-10-11(15-6-14-10)5-9(8)13-2/h4-5,7H,3,6,12H2,1-2H3
| Molecular Formula | C11H15NO3 |
| Molecular Weight | 209.2417 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 12:11:13 UTC 2023
by
admin
on
Sat Dec 16 12:11:13 UTC 2023
|
| Record UNII |
TG0B6ER184
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
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| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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WIKIPEDIA |
PiHKAL
Created by
admin on Sat Dec 16 12:11:14 UTC 2023 , Edited by admin on Sat Dec 16 12:11:14 UTC 2023
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WIKIPEDIA |
Designer-drugs-MMDA-2
Created by
admin on Sat Dec 16 12:11:14 UTC 2023 , Edited by admin on Sat Dec 16 12:11:14 UTC 2023
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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DTXSID20903968
Created by
admin on Sat Dec 16 12:11:14 UTC 2023 , Edited by admin on Sat Dec 16 12:11:14 UTC 2023
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PRIMARY | |||
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MMDA-2
Created by
admin on Sat Dec 16 12:11:14 UTC 2023 , Edited by admin on Sat Dec 16 12:11:14 UTC 2023
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PRIMARY | |||
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23693-18-7
Created by
admin on Sat Dec 16 12:11:14 UTC 2023 , Edited by admin on Sat Dec 16 12:11:14 UTC 2023
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PRIMARY | |||
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90966
Created by
admin on Sat Dec 16 12:11:14 UTC 2023 , Edited by admin on Sat Dec 16 12:11:14 UTC 2023
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PRIMARY | |||
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TG0B6ER184
Created by
admin on Sat Dec 16 12:11:14 UTC 2023 , Edited by admin on Sat Dec 16 12:11:14 UTC 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ENANTIOMER -> RACEMATE |
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SALT/SOLVATE -> PARENT |
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ENANTIOMER -> RACEMATE |
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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