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=CC=C2OC(F)(F)OC2=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
Sat Dec 16 10:41:43 GMT 2023
by
admin
on
Sat Dec 16 10:41:43 GMT 2023
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Record UNII |
8Q2ANL037S
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Record Status |
Validated (UNII)
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Record Version |
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-
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Common Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
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WIKIPEDIA |
Designer-drugs-Difluoromethylenedioxyamphetamine
Created by
admin on Sat Dec 16 10:41:43 GMT 2023 , Edited by admin on Sat Dec 16 10:41:43 GMT 2023
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Code System | Code | Type | Description | ||
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910393-51-0
Created by
admin on Sat Dec 16 10:41:43 GMT 2023 , Edited by admin on Sat Dec 16 10:41:43 GMT 2023
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PRIMARY | |||
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8Q2ANL037S
Created by
admin on Sat Dec 16 10:41:43 GMT 2023 , Edited by admin on Sat Dec 16 10:41:43 GMT 2023
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PRIMARY | |||
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DiFMDA
Created by
admin on Sat Dec 16 10:41:43 GMT 2023 , Edited by admin on Sat Dec 16 10:41:43 GMT 2023
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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. | ||
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57467735
Created by
admin on Sat Dec 16 10:41:43 GMT 2023 , Edited by admin on Sat Dec 16 10:41:43 GMT 2023
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PRIMARY | |||
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DTXSID10726729
Created by
admin on Sat Dec 16 10:41:43 GMT 2023 , Edited by admin on Sat Dec 16 10:41:43 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |