Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H17NO2 |
| Molecular Weight | 219.2796 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC2=C(OC=C2CCN(C)C)C=C1
InChI
InChIKey=WBPQJTBOQCCTFX-UHFFFAOYSA-N
InChI=1S/C13H17NO2/c1-14(2)7-6-10-9-16-13-5-4-11(15-3)8-12(10)13/h4-5,8-9H,6-7H2,1-3H3
| Molecular Formula | C13H17NO2 |
| Molecular Weight | 219.2796 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:15:29 GMT 2023
by
admin
on
Sat Dec 16 10:15:29 GMT 2023
|
| Record UNII |
9JXZ3RM7Y9
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
WIKIPEDIA |
Designer-drugs-Dimemebfe
Created by
admin on Sat Dec 16 10:15:29 GMT 2023 , Edited by admin on Sat Dec 16 10:15:29 GMT 2023
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
9JXZ3RM7Y9
Created by
admin on Sat Dec 16 10:15:29 GMT 2023 , Edited by admin on Sat Dec 16 10:15:29 GMT 2023
|
PRIMARY | |||
|
DTXSID80161481
Created by
admin on Sat Dec 16 10:15:29 GMT 2023 , Edited by admin on Sat Dec 16 10:15:29 GMT 2023
|
PRIMARY | |||
|
Dimemebfe
Created by
admin on Sat Dec 16 10:15:29 GMT 2023 , Edited by admin on Sat Dec 16 10:15:29 GMT 2023
|
PRIMARY | Dimemebfe (5-MeO-BFE) is a recreational drug[1] and research chemical. It acts as an agonist for the 5-HT1A and 5-HT2 family of serotonin receptors. It is related in structure to the psychedelic tryptamine derivative 5-MeO-DMT, but with the indole nitrogen replaced by oxygen, making dimemebfe a benzofuran derivative. It is several times less potent as a serotonin agonist than 5-MeO-DMT and with relatively more activity at 5-HT1A, but still shows strongest effects at the 5-HT2 family of receptors. | ||
|
140853-58-3
Created by
admin on Sat Dec 16 10:15:29 GMT 2023 , Edited by admin on Sat Dec 16 10:15:29 GMT 2023
|
PRIMARY | |||
|
126589
Created by
admin on Sat Dec 16 10:15:29 GMT 2023 , Edited by admin on Sat Dec 16 10:15:29 GMT 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
