Thiopropamine | |
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Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C7H11NS[1] |
Molecular mass | 141.24 g/mol[1] |
Predicted LogP | 1.8[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 1-thiophen-2-ylpropan-2-amine[1] |
SMILES | CC(CC1=CC=CS1)N[1] |
InChI | InChI=1S/C7H11NS/c1-6(8)5-7-3-2-4-9-7/h2-4,6H,5,8H2,1H3[1] |
InChIKey | NYVQQTOGYLBBDQ-UHFFFAOYSA-N[1] |
Dosing |
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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 cycloalkylethylamine class.
Chemistry
Stereochemistry
(RS)-Thiopropamine is a racemic mixture of the optical stereoisomers
Subjective effects
Physical effects [] |
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Cognitive effects [] |
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