Anodyne

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Clobenzorex
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
[]
Hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
[]
Conformer structure via JSmol
Physical properties
[]
259.77 g/mol [1]
4.3 [1]
Structural Identifiers
[]
C16H18ClN [1]
(2S)-N-[(2-chlorophenyl)methyl]-1-phenylpropan-2-amine [1]
C[C@@H](CC1=CC=CC=C1)NCC2=CC=CC=C2Cl [1]
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]
InChIKeyLRXXRIXDSAEIOR-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.

 []

Clobenzorex is a absolute mixture

Pharmacology

Clobenzorex acts as a for:

Active metabolites
 []
Dextroamphetamine Generated by the Chemistry Development Kit (http://github.com/cdk)

Subjective effects []

See also []

  • Substituted amphetamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 735998, Clobenzorex. Accessed July 19, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/735998

    2. 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