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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
Structure of 2-FLUOROAMPHETAMINE

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

HIDE SMILES / InChI

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 Sat Dec 16 11:04:49 UTC 2023
Edited
by admin
on Sat Dec 16 11:04:49 UTC 2023
Record UNII
V8Q7K3989D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-FLUOROAMPHETAMINE
Systematic Name English
1-(2-FLUOROPHENYL)-2-PROPYLAMINE
Systematic Name English
PHENETHYLAMINE, O-FLUORO-.ALPHA.-METHYL-
Systematic Name English
2-FLUORO-.ALPHA.-METHYLBENZENEETHANAMINE
Systematic Name English
BENZENEETHANAMINE, 2-FLUORO-.ALPHA.-METHYL-
Systematic Name English
2-FA
Common Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-2-FA
Created by admin on Sat Dec 16 11:04:49 UTC 2023 , Edited by admin on Sat Dec 16 11:04:49 UTC 2023
Code System Code Type Description
CAS
1716-60-5
Created by admin on Sat Dec 16 11:04:49 UTC 2023 , Edited by admin on Sat Dec 16 11:04:49 UTC 2023
PRIMARY
WIKIPEDIA
2-FLUOROAMPHETAMINE
Created by admin on Sat Dec 16 11:04:49 UTC 2023 , Edited by admin on Sat Dec 16 11:04:49 UTC 2023
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.
SMS_ID
300000028188
Created by admin on Sat Dec 16 11:04:49 UTC 2023 , Edited by admin on Sat Dec 16 11:04:49 UTC 2023
PRIMARY
PUBCHEM
121531
Created by admin on Sat Dec 16 11:04:49 UTC 2023 , Edited by admin on Sat Dec 16 11:04:49 UTC 2023
PRIMARY
FDA UNII
V8Q7K3989D
Created by admin on Sat Dec 16 11:04:49 UTC 2023 , Edited by admin on Sat Dec 16 11:04:49 UTC 2023
PRIMARY
EPA CompTox
DTXSID30938009
Created by admin on Sat Dec 16 11:04:49 UTC 2023 , Edited by admin on Sat Dec 16 11:04:49 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY