N-Methylbupropion | |
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Molecular structure via molpic based on CDK |
Rotamer [] | |
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Physical properties [] | |
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Molecular mass | 253.77 g/mol [1] |
Predicted LogP | 3.7 [1] |
Structural Identifiers [] | |
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Molecular formula | C14H20ClNO [1] |
IUPAC name | 2-[tert-butyl(methyl)amino]-1-(3-chlorophenyl)propan-1-one [1] |
SMILES | CC(C(=O)C1=CC(=CC=C1)Cl)N(C)C(C)(C)C [1] |
InChI | InChI=1S/C14H20ClNO/c1-10(16(5)14(2,3)4)13(17)11-7-6-8-12(15)9-11/h6-10H,1-5H3 [1] |
InChIKey | BJLKZFUZNNATGZ-UHFFFAOYSA-N [1] |
N-Methylbupropion
N-Methylbupropion (also known as N-Methylbupropion, N-methyl-bupropion, 2-(tert-butyl(methyl)amino)-1-(3-chlorophenyl)propan-1-one or 2-(N-Methyl-N-tert-butylamino)-3''-chloropropiophenone) is a stimulant substance of the amphetamine class.
Chemistry
Stereochemistry []
N-Methylbupropion is a racemic mixture of the enantiomers
Stereoisomers |
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Pharmacology
N-Methylbupropion acts as a prodrug for:
Active metabolites [] |
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Subjective effects
See also []
External links []
References []
National Center for Biotechnology Information. PubChem Compound Summary for CID 20695745, N-Methylbupropion. Accessed August 31, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/20695745