Details
Stereochemistry | RACEMIC |
Molecular Formula | C9H12FN |
Molecular Weight | 153.1967 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(N)CC1=C(F)C=CC=C1
InChI
InChIKey=GDSXNLDTQFFIEU-UHFFFAOYSA-N
InChI=1S/C9H12FN/c1-7(11)6-8-4-2-3-5-9(8)10/h2-5,7H,6,11H2,1H3
Molecular Formula | C9H12FN |
Molecular Weight | 153.1967 |
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 11:04:49 GMT 2023
by
admin
on
Sat Dec 16 11:04:49 GMT 2023
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Record UNII |
V8Q7K3989D
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Record Status |
Validated (UNII)
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Record Version |
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-
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WIKIPEDIA |
Designer-drugs-2-FA
Created by
admin on Sat Dec 16 11:04:49 GMT 2023 , Edited by admin on Sat Dec 16 11:04:49 GMT 2023
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Code System | Code | Type | Description | ||
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1716-60-5
Created by
admin on Sat Dec 16 11:04:49 GMT 2023 , Edited by admin on Sat Dec 16 11:04:49 GMT 2023
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PRIMARY | |||
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2-FLUOROAMPHETAMINE
Created by
admin on Sat Dec 16 11:04:49 GMT 2023 , Edited by admin on Sat Dec 16 11:04:49 GMT 2023
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PRIMARY | 2-Fluoroamphetamine (2-FA) is a stimulant drug from the amphetamine family which has been sold as a designer drug. 2-Fluoroamphetamine differs from 3- and 4-fluoroamphetamine in the position of the fluorine atom on the aromatic ring, making them positional isomers of one another. The replacement of a hydrogen atom with a fluorine atom in certain compounds to facilitate passage through the blood?brain barrier, as is desirable in central nervous system pharmaceutical agents, is a common practice due to the corresponding increase in lipophilicity granted by the substitute. | ||
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300000028188
Created by
admin on Sat Dec 16 11:04:49 GMT 2023 , Edited by admin on Sat Dec 16 11:04:49 GMT 2023
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121531
Created by
admin on Sat Dec 16 11:04:49 GMT 2023 , Edited by admin on Sat Dec 16 11:04:49 GMT 2023
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V8Q7K3989D
Created by
admin on Sat Dec 16 11:04:49 GMT 2023 , Edited by admin on Sat Dec 16 11:04:49 GMT 2023
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DTXSID30938009
Created by
admin on Sat Dec 16 11:04:49 GMT 2023 , Edited by admin on Sat Dec 16 11:04:49 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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SALT/SOLVATE -> PARENT | |||
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ENANTIOMER -> RACEMATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |