Anodyne

RTI-121

Molecular structure via molpic based on CDK

Physical properties []
Molecular mass	413.3 g/mol ^[1]
Predicted LogP	4.1 ^[1]

Structural Identifiers []
Molecular formula	C₁₈H₂₄INO₂ ^[1]
IUPAC name	propan-2-yl (1R,2S,3S)-3-(4-iodophenyl)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylate ^[1]
SMILES	CC(C)OC(=O)[C@@H]1[C@H]2CCC(N2C)C[C@@H]1C3=CC=C(C=C3)I ^[1]
InChI	InChI=1S/C18H24INO2/c1-11(2)22-18(21)17-15(12-4-6-13(19)7-5-12)10-14-8-9-16(17)20(14)3/h4-7,11,14-17H,8-10H2,1-3H3/t14?,15-,16-,17+/m1/s1 ^[1]
InChIKey	ZAQLTGAFVMGUMB-IFFAKLHKSA-N ^[1]

2β-Carboisopropoxy-3β-(4-iodophenyl)tropane

2β-Carboisopropoxy-3β-(4-iodophenyl)tropane is a stimulant substance of the phenyltropane class.

Chemistry

Stereochemistry []

2β-Carboisopropoxy-3β-(4-iodophenyl)tropane is a achiral mixture

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

See also []

Substituted phenyltropanes

External links []

References []

National Center for Biotechnology Information. PubChem Compound Summary for CID 122190, 3beta-(4-Iodophenyl)tropan-2beta-carboxylic acid isopropyl ester. Accessed November 11, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/122190