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5-Chloro-β-keto-methiopropamine
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic
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Physical properties
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Molecular mass203.69 g/mol [1]
Predicted LogP2.6 [1]
Structural Identifiers
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Molecular formulaC8H10ClNOS [1]
IUPAC name1-(5-chlorothiophen-2-yl)-2-(methylamino)propan-1-one [1]
SMILESCC(C(=O)C1=CC=C(S1)Cl)NC [1]
InChIInChI=1S/C8H10ClNOS/c1-5(10-2)8(11)6-3-4-7(9)12-6/h3-5,10H,1-2H3 [1]
InChIKeyVTSPXQPERGVFBV-UHFFFAOYSA-N [1]
Dosing

5-Chloro-β-keto-methiopropamine

5-Chloro-β-keto-methiopropamine (also known as 1-(5-Chloro-2-thienyl)-2-(methylamino)-1-propanone or 1-Propanone, 1-(5-chloro-2-thienyl)-2-(methylamino)-) is a stimulant substance of the thiopropamine class.

Chemistry

Stereochemistry []

5-Chloro-β-keto-methiopropamine is a racemic mixture of the optical stereoisomers:

Stereoisomers
(+)-5-Chloro-β-keto-methiopropamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(-)-5-Chloro-β-keto-methiopropamineGenerated by the Chemistry Development Kit (http://github.com/cdk)

Subjective effects
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See also []

  • Substituted thiopropamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 82282703, 5-Chloro-β-keto-methiopropamine. Accessed July 13, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/82282703

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 5-Chloro-β-keto-methiopropamine. UNII: 4F8W3K5FA4. Global Substance Registration System. Accessed July 13, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/4F8W3K5FA4