Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H11F2NO2 |
| Molecular Weight | 215.1966 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(N)CC1=CC2=C(OC(F)(F)O2)C=C1
InChI
InChIKey=BHDXKBALNFHXDV-UHFFFAOYSA-N
InChI=1S/C10H11F2NO2/c1-6(13)4-7-2-3-8-9(5-7)15-10(11,12)14-8/h2-3,5-6H,4,13H2,1H3
| Molecular Formula | C10H11F2NO2 |
| Molecular Weight | 215.1966 |
| 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
Mon Mar 31 23:23:53 GMT 2025
by
admin
on
Mon Mar 31 23:23:53 GMT 2025
|
| Record UNII |
8Q2ANL037S
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
WIKIPEDIA |
Designer-drugs-Difluoromethylenedioxyamphetamine
Created by
admin on Mon Mar 31 23:23:53 GMT 2025 , Edited by admin on Mon Mar 31 23:23:53 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
910393-51-0
Created by
admin on Mon Mar 31 23:23:53 GMT 2025 , Edited by admin on Mon Mar 31 23:23:53 GMT 2025
|
PRIMARY | |||
|
8Q2ANL037S
Created by
admin on Mon Mar 31 23:23:53 GMT 2025 , Edited by admin on Mon Mar 31 23:23:53 GMT 2025
|
PRIMARY | |||
|
DiFMDA
Created by
admin on Mon Mar 31 23:23:53 GMT 2025 , Edited by admin on Mon Mar 31 23:23:53 GMT 2025
|
PRIMARY | Difluoromethylenedioxyamphetamine (DiFMDA) is a substituted derivative of methylenedioxyamphetamine (MDA), which was developed by Daniel Trachsel and coworkers, along with the corresponding fluorinated derivatives of MDMA, MDEA, BDB and MBDB, with the aim of finding a non-neurotoxic drug able to be used as a less harmful substitute for entactogenic drugs such as MDMA. | ||
|
57467735
Created by
admin on Mon Mar 31 23:23:53 GMT 2025 , Edited by admin on Mon Mar 31 23:23:53 GMT 2025
|
PRIMARY | |||
|
DTXSID10726729
Created by
admin on Mon Mar 31 23:23:53 GMT 2025 , Edited by admin on Mon Mar 31 23:23:53 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ENANTIOMER -> RACEMATE | |||
|
ENANTIOMER -> RACEMATE |
