2-Chloromethcathinone

2-CMC

Molecular structure via molpic based on CDK

Physical properties []
Molecular mass	197.66 g/mol ^[1]
Predicted LogP	2.1 ^[1]

Structural Identifiers []
Molecular formula	C₁₀H₁₂ClNO ^[1]
IUPAC name	1-(2-chlorophenyl)-2-(methylamino)propan-1-one ^[1]
SMILES	CC(C(=O)C1=CC=CC=C1Cl)NC ^[1]
InChI	InChI=1S/C10H12ClNO/c1-7(12-2)10(13)8-5-3-4-6-9(8)11/h3-7,12H,1-2H3 ^[1]
InChIKey	UHVGPEBZWPKWNT-UHFFFAOYSA-N ^[1]

2-Chloromethcathinone (also known as 2-Cmc, 1-(2-Chlorophenyl)-2-(methylamino)-1-propanone, 1-Propanone, 1-(2-chlorophenyl)-2-(methylamino)- or NS00097768) is a stimulant substance of the cathinone class.

Chemistry

Stereochemistry []

2-Chloromethcathinone is a racemic mixture of the enantiomers.

Stereoisomerism
(R)-2-Chloromethcathinone (S)-2-Chloromethcathinone
Stereoisomer enumberation with rdkit

Subjective effects []

class / Stimulant

Physical effects
Abnormal heartbeat Appetite suppression Dehydration Dry mouth Increased blood pressure Increased heart rate Increased libido Restless legs Shakiness Stamina enhancement Stimulation Teeth grinding Vasoconstriction

Cognitive effects
Analysis enhancement Cognitive euphoria Compulsive redosing Disinhibition Ego inflation Focus enhancement Increased music appreciation Mania Motivation enhancement Suggestibility suppression Thought acceleration Wakefulness

External links []

References []

National Center for Biotechnology Information. PubChem Compound Summary for CID 112693018, 2-Chloromethcathinone. Accessed October 15, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/112693018
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2-Chloromethcathinone. UNII: 843M5D2FGG. Global Substance Registration System. Accessed October 15, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/843M5D2FGG

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