Clobenzorex

Salts []
Hydrochloride

Molecular structure via molpic based on CDK

Physical properties []
Molecular mass	259.77 g/mol ^[1]
Predicted LogP	4.3 ^[1]

Structural Identifiers []
Molecular formula	C₁₆H₁₈ClN ^[1]
IUPAC name	(2S)-N-[(2-chlorophenyl)methyl]-1-phenylpropan-2-amine ^[1]
SMILES	C[C@@H](CC1=CC=CC=C1)NCC2=CC=CC=C2Cl ^[1]
InChI	InChI=1S/C16H18ClN/c1-13(11-14-7-3-2-4-8-14)18-12-15-9-5-6-10-16(15)17/h2-10,13,18H,11-12H2,1H3/t13-/m0/s1 ^[1]
InChIKey	LRXXRIXDSAEIOR-ZDUSSCGKSA-N ^[1]

Clobenzorex

Clobenzorex (also known as Clobenzorexum, SD 271-12, SD-27112, SD-271-12, A08AA08, N-(o-chlorobenzyl)-α-methylphenethylamine, ((2-chlorophenyl)methyl)((2S)-1-phenylpropan-2-yl)amine, 236-434-4, N-(o-Chlorobenzyl)-α-methylphenethylamine or DB13561) is a prodrug and stimulant substance of the amphetamine class.

Chemistry

Salts []

Clobenzorex is typically found in the form of its hydrochloride salt.

Stereochemistry []

Clobenzorex is a absolute mixture

Pharmacology

Clobenzorex acts as a prodrug for:

Active metabolites []
Dextroamphetamine

Subjective effects []

Physical effects
Abnormal heartbeat Appetite suppression Dehydration Dry mouth Increased blood pressure Increased heart rate Increased libido Restless legs Shakiness Stamina enhancement Stimulation Teeth grinding Vasoconstriction

Cognitive effects
Analysis enhancement Cognitive euphoria Compulsive redosing Disinhibition Ego inflation Focus enhancement Increased music appreciation Mania Motivation enhancement Suggestibility suppression Thought acceleration Wakefulness

External links []

References []

National Center for Biotechnology Information. PubChem Compound Summary for CID 735998, Clobenzorex. Accessed July 19, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/735998
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Clobenzorex. UNII: 4A5352XI2A. Global Substance Registration System. Accessed July 19, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/4A5352XI2A

Anodyne