Anodyne

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5-MAPB
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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189.25 g/mol [1]
2.6 [1]
Structural Identifiers
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C12H15NO [1]
1-(1-benzofuran-5-yl)-N-methylpropan-2-amine [1]
CC(CC1=CC2=C(C=C1)OC=C2)NC [1]
InChI=1S/C12H15NO/c1-9(13-2)7-10-3-4-12-11(8-10)5-6-14-12/h3-6,8-9,13H,7H2,1-2H3 [1]
InChIKeyZOVRTIPCNFERHY-UHFFFAOYSA-N [1]

5-(N-methyl-2-aminopropyl)benzofuran

5-(N-methyl-2-aminopropyl)benzofuran (also known as 5-(N-methyl-2-aminopropyl)benzofuran, 1-(benzofuran-5-yl)-N-Methylpropan-2-aMine, 5-MAPB, 5-(N-Methyl-2-aminopropyl)benzofuran, 5-Benzofuranethanamine, N,α-dimethyl-, 5-Benzofuranethanamine, n,α-dimethyl- or 6-MAPB (N-methyl (6-(2-aminopropyl)benzofuran))) is a substance of the amphetamine class.

Chemistry

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5-(N-methyl-2-aminopropyl)benzofuran is a racemic mixture of the

Stereoisomers
(R)-5-(N-methyl-2-aminopropyl)benzofuranGenerated by the Chemistry Development Kit (http://github.com/cdk)
(S)-5-(N-methyl-2-aminopropyl)benzofuranGenerated by the Chemistry Development Kit (http://github.com/cdk)
Anodyne Usernotes
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magnus / 5-(N-methyl-2-aminopropyl)benzofuran via Oral at 150-220mg oral
  • increased ; slight visuals; less /calmer experience than MDMA; strong feeling of love; music enhancement; rolling‘/vibrating eyes; much better suited than MDMA for rolling at home

See also []

  • Substituted amphetamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 102336592, 5-(N-methyl-2-aminopropyl)benzofuran. Accessed September 1, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/102336592

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 5-(N-methyl-2-aminopropyl)benzofuran. UNII: XW34GUY2OY. Global Substance Registration System. Accessed September 1, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/XW34GUY2OY