Propylone | |
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Salts [] | |
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Propylone hydrochloride | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C13H17NO3[1] |
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Molecular mass | 235.28 g/mol[1] |
Predicted LogP | 2.3[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 1-(1,3-benzodioxol-5-yl)-2-(propylamino)propan-1-one[1] |
SMILES | CCCNC(C)C(=O)C1=CC2=C(C=C1)OCO2[1] |
InChI | InChI=1S/C13H17NO3/c1-3-6-14-9(2)13(15)10-4-5-11-12(7-10)17-8-16-11/h4-5,7,9,14H,3,6,8H2,1-2H3[1] |
InChIKey | YFVKHKCZBSGZPE-UHFFFAOYSA-N[1] |
Dosing |
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Propylone
Propylone (also known as Prone, BK-3,4-mdpa, 3,4-Methylenedioxy-n-propylcathinone, Propyl-3,4-methylenedioxycathinone, (2S)-1-(1,3-Benzodioxol-5-yl)-2-(propylamino)-1-propanone, 1-Propanone, 1-(1,3-benzodioxol-5-yl)-2-(propylamino)-, (2S)- or 1-Propanone, 1-(1,3-benzodioxol-5-yl)-2-(propylamino)-, (S)-) is a substance of the cathinone class.
Chemistry
Propylone is typically found in the form of its hydrochloride salt.
Stereochemistry
(RS)-Propylone is a racemic mixture of the optical stereoisomers