Anodyne

2-Br-2'-Oxo-PCM, 2-Br-DCK
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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282.18 g/mol [1]
2.2 [1]
Structural Identifiers
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C13H16BrNO [1]
2-(2-bromophenyl)-2-(methylamino)cyclohexan-1-one [1]
CNC1(CCCCC1=O)C2=CC=CC=C2Br [1]
InChI=1S/C13H16BrNO/c1-15-13(9-5-4-8-12(13)16)10-6-2-3-7-11(10)14/h2-3,6-7,15H,4-5,8-9H2,1H3 [1]
InChIKeyXPMMBFIMXKSQIQ-UHFFFAOYSA-N [1]

Bromoketamine

Bromoketamine (also known as 2-(2-bromophenyl)-2-(methylamino)cyclohexanone, 2-Bromo deschloroketamine, 2-Bromodeschloroketamine, Cyclohexanone, 2-(2-bromophenyl)-2-(methylamino)-, RefChem:197694, 2-(2-bromophenyl)-2-(methylamino)-cyclohexanone or 2(o-bromophenyl)-2-methylaminocyclohexanone) is a substance of the arylcyclohexylamine class.

Chemistry

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Bromoketamine is a racemic mixture of the

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

Legal status []

  • Canada: Bromoketamine is a Schedule I substance.
  • Germany: Bromoketamine is a Neuer-Psychoaktiver-Stoff under the "Neue-psychoaktive-Stoffe-Gesetz (NpSG)".
  • United Kingdom: Bromoketamine is a Class B substance.

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 71588007, Bromoketamine. Accessed September 6, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/71588007

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Bromoketamine. UNII: BG9ADQ6XT9. Global Substance Registration System. Accessed September 6, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/BG9ADQ6XT9