Anodyne

Collapse all
Toggle theme
Thiopropamine
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic
Enable javascript to view conformer structure via 3Dmol.js
Physical properties
[]
Molecular mass141.24 g/mol [1]
Predicted LogP1.8 [1]
Structural Identifiers
[]
Molecular formulaC7H11NS [1]
IUPAC name1-thiophen-2-ylpropan-2-amine [1]
SMILESCC(CC1=CC=CS1)N [1]
InChIInChI=1S/C7H11NS/c1-6(8)5-7-3-2-4-9-7/h2-4,6H,5,8H2,1H3 [1]
InChIKeyNYVQQTOGYLBBDQ-UHFFFAOYSA-N [1]
Dosing

Thiopropamine

Thiopropamine (also known as 2-(2-Aminopropyl)thiophene, 2-Thiopheneethanamine, α-methyl-, 1-(2-Thienyl)-2-propanamine, 1-(Thien-2-yl)propan-2-amine, 1-Methyl-2-(thien-2-yl)ethylamine, (1-Methyl-2-(thiophen-2-yl)ethyl)amine, α-Methyl-2-thiopheneethanamine, α-Methyl-2-thiopheneethylamine, 1-(3,3-diphenylpropyl)amino-3-phenylthiopropane or 1-(thiophen-2-yl)propan-2-amine) is a stimulant substance of the thiopropamine class.

Chemistry

Stereochemistry []

Thiopropamine is a racemic mixture of the optical stereoisomers

Subjective effects
 []
[]
[]

See also []

  • Substituted thiopropamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 6484133, Thiopropamine. Accessed July 13, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/6484133

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Thiopropamine. UNII: N60H4ZDD14. Global Substance Registration System. Accessed July 13, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/N60H4ZDD14