{"Abbreviation":["4-CMC"],"Aliases":["Clephedrone","4-cmc","4-Chloromethcathinone","Dtxsid201014163","Dtxcid501436704","Unii-ptayyyzmmt","1-(4-Chlorophenyl)-2-(methylamino)propan-1-one","para-Chloro-N-methyl-cathinone","4-Chloromethcathinone hydrochloride","Chloromethcathinone","1-(4-chlorophenyl)-2-(methylamino)-1-propanone","Schembl21271211","AZB84386","NS00017372","1-(4-Chlorophenyl)-2-methylaminopropan-1-one","C22721","1-Propanone, 1-(4-chlorophenyl)-2-(methylamino)-"],"CAS":"1225843-86-6","ChemicalClasses":["cathinone"],"Chirality":"racemic","Classes":["Stimulant"],"EliminationHalfLife":"","Erowid Experience Reports":[],"Esters":[],"European Community (EC) Number":"822-720-1","Formating":[],"HMDB ID":"HMDB0250318","HeavyAtomCount":13,"IUPACName":"1-(4-chlorophenyl)-2-(methylamino)propan-1-one","InChI":"InChI=1S/C10H12ClNO/c1-7(12-2)10(13)8-3-5-9(11)6-4-8/h3-7,12H,1-2H3","InChIKey":"UEJBEYOXRNGPEI-UHFFFAOYSA-N","MeSH Headers":[{"Id":"M000611658","Link":"https://id.nlm.nih.gov/mesh/M000611658.html","Name":"clephedrone","Ref":21},{"Id":"DescTree","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":"MeSH Tree","Ref":23},{"Id":"PubMed from MeSH","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":null,"Ref":33}],"MolecularFormula":"C\u003csub\u003e10\u003c/sub\u003eH\u003csub\u003e12\u003c/sub\u003eClNO","MolecularWeight":"197.66 g/mol","Opticalactivity":"( + / - )","PubChemId":82100418,"Record Description":["4-Chloromethcathinone (also known as 4-CMC and Clephedrone) is a stimulant drug of the cathinone class that has been sold online as a designer drug. Clephedrone is an Anlage I controlled drug in Germany. Sweden's public health agency suggested classifying 4-Chloromethcathinone (klefedron) as illegal narcotic on June 1, 2015. As of October 2015 4-CMC is a controlled substance in China.","Wikipedia|List of designer drugs|Stimulants|Cathinones"],"Records":{"UNII":{"Impurities":[]}},"RefChem":"126936","RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/4-Chloromethcathinone","Name":"Clephedrone","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q21098974","Name":"Clephedrone","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/82100418","Name":"Clephedrone","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=1225843-86-6","Name":"Clephedrone","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0250318","Name":"Clephedrone","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C22721","Name":"Clephedrone","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/PTAYYYZMMT","Name":"Clephedrone","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID201014163","Name":"Clephedrone","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 82100418, Clephedrone. Accessed May 4, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/82100418\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/82100418\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Clephedrone. UNII: PTAYYYZMMT. Global Substance Registration System. Accessed May 4, 2026. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/PTAYYYZMMT\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/PTAYYYZMMT\u003c/a\u003e"],"SMILES":"CC(C(=O)C1=CC=C(C=C1)Cl)NC","SaltData":[],"Salts":[],"Scheduling":[{"gov":"Brazil","ref":[],"schedule":"F2 substance"},{"gov":"Germany","ref":[],"schedule":"Anlage I substance"},{"gov":"United Kingdom","ref":[],"schedule":"Class B substance"},{"act":"Convention on Psychotropic Substances 1971","gov":"United Nations","ref":[],"schedule":"Schedule II drug"}],"StereoisomerData":[{"ChemicalClasses":["cathinone"],"SMILES":"CN[C@H](C)C(=O)C1=CC=C(Cl)C=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 98.787 52.04\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#3050f8\" stroke=\"#000\" 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4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578zM86.355 15.31h-.619v-2.286h-2.513v2.286h-.613v-4.9h.613v2.072h2.513V10.41h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#1ff01f\" d=\"m6.875 47.927 5.842-3.373\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m81.398 20.142-5.023 2.899M81.398 20.142l-5.023 2.899M87.704 20.142l5.022 2.899M87.704 20.142l5.022 2.899\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Subjective Effects":{"Cognitive Effects":["Analysis enhancement","Ego inflation","Focus enhancement","Increased music appreciation","Motivation enhancement","Thought acceleration","Wakefulness","Disinhibition","Suggestibility suppression","Cognitive euphoria","Compulsive redosing","Mania"],"Physical Effects":["Increased libido","Stamina enhancement","Stimulation","Appetite suppression","Dehydration","Dry mouth","Restless legs","Shakiness","Teeth grinding","Abnormal heartbeat","Increased blood pressure","Increased heart rate","Vasoconstriction"],"Visual Effects":[]},"Title":"Clephedrone","UNII":"PTAYYYZMMT","Wikidata":"Q21098974","Wikipedia":"4-Chloromethcathinone","XLogP":2.2}