Rimiterol

Rimiterol

Molecular structure via molpic based on CDK

Rotamer []

Conformer structure via 3Dmol.js

Physical properties []
Molecular mass	223.27 g/mol ^[1]
Predicted LogP	0.8 ^[1]

Structural Identifiers []
Molecular formula	C₁₂H₁₇NO₃ ^[1]
IUPAC name	4-[hydroxy(piperidin-2-yl)methyl]benzene-1,2-diol ^[1]
SMILES	C1CCNC(C1)C(C2=CC(=C(C=C2)O)O)O ^[1]
InChI	InChI=1S/C12H17NO3/c14-10-5-4-8(7-11(10)15)12(16)9-3-1-2-6-13-9/h4-5,7,9,12-16H,1-3,6H2 ^[1]
InChIKey	IYMMESGOJVNCKV-UHFFFAOYSA-N ^[1]

Rimiterol (also known as NSC289336, erythro-3,4-Dihydroxyphenyl-2-piperidylcarbinol, Chembl88055, Schembl3130599, Schembl29443594, Chebi:134917, Nci60_002370 or 4-(hydroxy(2-piperidinyl)methyl)-1,2-benzenediol) is a sympathomimetic substance of the 2-benzylpiperidine class.

Chemistry

Stereochemistry []

Rimiterol is a racemic mixture of the diastereomers.

Stereoisomerism
(4R,6S)-Rimiterol (4S,6S)-Rimiterol (4R,6R)-Rimiterol (4S,6R)-Rimiterol
Stereoisomer enumberation with rdkit

Subjective effects []

class / Sympathomimetic

Physical effects
Abnormal heartbeat Dehydration Dry mouth Increased blood pressure Increased heart rate Restless legs Shakiness Stamina enhancement Vasoconstriction

Cognitive effects
Thought acceleration Wakefulness

Legal status []

Australia: Rimiterol is a S4 substance.

External links []

References []

National Center for Biotechnology Information. PubChem Compound Summary for CID 431097, NSC289336. Accessed May 8, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/431097

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