Anodyne

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2-MeO-DCK
Generated by the Chemistry Development Kit (http://github.com/cdk)
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Methoxyketamine hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
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Physical properties
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233.31 g/mol [1]
1.5 [1]
Structural Identifiers
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C14H19NO2 [1]
2-(2-methoxyphenyl)-2-(methylamino)cyclohexan-1-one [1]
CNC1(CCCCC1=O)C2=CC=CC=C2OC [1]
InChI=1S/C14H19NO2/c1-15-14(10-6-5-9-13(14)16)11-7-3-4-8-12(11)17-2/h3-4,7-8,15H,5-6,9-10H2,1-2H3 [1]
InChIKeyOYAUVHORXFUVAJ-UHFFFAOYSA-N [1]

Methoxyketamine

Methoxyketamine (also known as 2-(2-Methoxyphenyl)-2-(methylamino)cyclohexanone, 2-methoxyketamine, 2-Methoxy ketamine, 2-2-Methoxyphenyl-2-methylamino cyclohexanone, Cyclohexanone, 2-(2-methoxyphenyl)-2-(methylamino)- or Cyclohexanone, 2-(o-methoxyphenyl)-2-(methylamino)-) is a substance of the arylcyclohexylamine class.

Chemistry

Salts []

Methoxyketamine is typically found in the form of its hydrochloride salt.

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Methoxyketamine is a racemic mixture of the

Stereoisomers
(R)-MethoxyketamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(S)-MethoxyketamineGenerated by the Chemistry Development Kit (http://github.com/cdk)

See also []

  • Substituted arylcyclohexylamines
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 57483650, Methoxyketamine. Accessed September 6, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/57483650

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Methoxyketamine. UNII: U4I8JIS24N. Global Substance Registration System. Accessed September 6, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/U4I8JIS24N