{"Abbreviation":["2-CMC"],"Aliases":["2-Cmc","1-(2-Chlorophenyl)-2-(methylamino)-1-propanone","1-Propanone, 1-(2-chlorophenyl)-2-(methylamino)-","NS00097768"],"CAS":"692720-34-6","ChemicalClasses":["cathinone"],"Chirality":"racemic","Classes":["Stimulant"],"DTXSID":"301342727","Esters":[],"Formating":[],"HeavyAtomCount":13,"IUPACName":"1-(2-chlorophenyl)-2-(methylamino)propan-1-one","InChI":"InChI=1S/C10H12ClNO/c1-7(12-2)10(13)8-5-3-4-6-9(8)11/h3-7,12H,1-2H3","InChIKey":"UHVGPEBZWPKWNT-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e10\u003c/sub\u003eH\u003csub\u003e12\u003c/sub\u003eClNO","MolecularWeight":"197.66 g/mol","Opticalactivity":"( + / - )","PD":"PD057778","PubChemId":112693018,"PubChemTitle":"2-Chloromethcathinone","Record Description":["Wikipedia|List of designer drugs|Stimulants|Cathinones"],"Records":{"UNII":{"Impurities":[]}},"RefChem":"197734","RefCount":2,"References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/112693018","Name":"2-Chloromethcathinone","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD057778","Name":"2-Chloromethcathinone","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=692720-34-6","Name":"2-Chloromethcathinone","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/843M5D2FGG","Name":"2-Chloromethcathinone","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID301342727","Name":"2-Chloromethcathinone","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 112693018, 2-Chloromethcathinone. Accessed October 15, 2026. \u003ca href='https://pubchem.ncbi.nlm.nih.gov/compound/112693018'\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/112693018\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2-Chloromethcathinone. UNII: 843M5D2FGG. Global Substance Registration System. Accessed October 15, 2026. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/843M5D2FGG\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/843M5D2FGG\u003c/a\u003e"],"SMILES":"CC(C(=O)C1=CC=CC=C1Cl)NC","SaltData":[],"Salts":[],"StereoisomerData":[{"ChemicalClasses":["cathinone"],"SMILES":"CN[C@H](C)C(=O)C1=CC=CC=C1Cl","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.407 52.032\"\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\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v53H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m80.301 26.013-9.914-5.724M63.824 20.286l-9.92 5.727\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M54.304 26.013h-.8M54.59 28.19h-1.372M54.876 30.367h-1.943M55.162 32.544h-2.515M55.447 34.721h-3.086M55.733 36.898h-3.658M56.019 39.075H51.79M56.305 41.253h-4.801\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.904 26.013-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M39.487 19.096V7.345M41.925 19.096V7.345\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M39.487 7.345v5.875M41.925 7.345v5.875\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.706 18.393-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.508 26.013-13.203-7.629M25.07 27.42 14.304 21.2\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.305 18.384-13.199 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.106 26.004.005 15.249M3.545 27.412l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.111 41.253 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.314 48.881 13.199-7.62M14.315 46.065l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.508 26.013.005 15.248M27.513 41.261l9.798 5.655\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M65.209 15.892h.911l2.215 4.185v-4.185h.661v5.001h-.911l-2.221-4.185v4.185h-.655zM65.209 10.32h.679v2.048h2.459V10.32h.672v5.001h-.672V12.94h-2.459v2.381h-.679z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M40.709 1.108q-.738 0-1.173.553-.428.548-.428 1.495 0 .946.428 1.494.435.547 1.173.547t1.167-.547q.428-.548.428-1.494 0-.947-.428-1.495-.429-.553-1.167-.553m0-.548q1.054 0 1.679.708.631.703.631 1.888 0 1.178-.631 1.887-.625.702-1.679.702t-1.685-.702q-.631-.703-.631-1.887t.631-1.888Q39.655.56 40.709.56\" class=\"atom\"/\u003e\u003cpath fill=\"#1ff01f\" stroke=\"none\" d=\"M42.727 46.763v.714q-.339-.321-.726-.476-.387-.161-.822-.161-.857 0-1.315.524-.453.524-.453 1.518 0 .988.453 1.512.458.524 1.315.524.435 0 .822-.155.387-.161.726-.476v.702q-.357.244-.756.363-.393.12-.833.12-1.137 0-1.792-.691-.649-.697-.649-1.899 0-1.209.649-1.899.655-.697 1.792-.697.446 0 .839.119.399.119.75.358m1.021-.596h.613v5.209h-.613z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.387 20.289 4.957 2.862M63.824 20.286l-4.96 2.864\" class=\"hi\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m37.311 46.916-4.899-2.828\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-2-Chloromethcathinone"},{"ChemicalClasses":["cathinone"],"SMILES":"CN[C@@H](C)C(=O)C1=CC=CC=C1Cl","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.407 52.032\"\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\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v53H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m80.301 26.013-9.914-5.724M63.824 20.286l-9.92 5.727\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M54.304 26.013h-.8l-2 15.24h4.801z\" class=\"bond\"/\u003e\u003cpath d=\"m53.904 26.013-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M39.487 19.096V7.345M41.925 19.096V7.345\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M39.487 7.345v5.875M41.925 7.345v5.875\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.706 18.393-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.508 26.013-13.203-7.629M25.07 27.42 14.304 21.2\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.305 18.384-13.199 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.106 26.004.005 15.249M3.545 27.412l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.111 41.253 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.314 48.881 13.199-7.62M14.315 46.065l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.508 26.013.005 15.248M27.513 41.261l9.798 5.655\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M65.209 15.892h.911l2.215 4.185v-4.185h.661v5.001h-.911l-2.221-4.185v4.185h-.655zM65.209 10.32h.679v2.048h2.459V10.32h.672v5.001h-.672V12.94h-2.459v2.381h-.679z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M40.709 1.108q-.738 0-1.173.553-.428.548-.428 1.495 0 .946.428 1.494.435.547 1.173.547t1.167-.547q.428-.548.428-1.494 0-.947-.428-1.495-.429-.553-1.167-.553m0-.548q1.054 0 1.679.708.631.703.631 1.888 0 1.178-.631 1.887-.625.702-1.679.702t-1.685-.702q-.631-.703-.631-1.887t.631-1.888Q39.655.56 40.709.56\" class=\"atom\"/\u003e\u003cpath fill=\"#1ff01f\" stroke=\"none\" d=\"M42.727 46.763v.714q-.339-.321-.726-.476-.387-.161-.822-.161-.857 0-1.315.524-.453.524-.453 1.518 0 .988.453 1.512.458.524 1.315.524.435 0 .822-.155.387-.161.726-.476v.702q-.357.244-.756.363-.393.12-.833.12-1.137 0-1.792-.691-.649-.697-.649-1.899 0-1.209.649-1.899.655-.697 1.792-.697.446 0 .839.119.399.119.75.358m1.021-.596h.613v5.209h-.613z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.387 20.289 4.957 2.862M63.824 20.286l-4.96 2.864\" class=\"hi\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m37.311 46.916-4.899-2.828\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-2-Chloromethcathinone"}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-2-Chloromethcathinone","(S)-2-Chloromethcathinone"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.407 52.032\"\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\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v53H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M53.904 41.253v-15.24M53.904 26.013l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M39.487 19.096V7.345M41.925 19.096V7.345\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M39.487 7.345v5.875M41.925 7.345v5.875\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.706 18.393-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.508 26.013-13.203-7.629M25.07 27.42 14.304 21.2\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.305 18.384-13.199 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.106 26.004.005 15.249M3.545 27.412l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.111 41.253 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.314 48.881 13.199-7.62M14.315 46.065l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.508 26.013.005 15.248M27.513 41.261l9.798 5.655M53.904 26.013l9.92-5.727M70.387 20.289l9.914 5.724\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M40.709 1.108q-.738 0-1.173.553-.428.548-.428 1.495 0 .946.428 1.494.435.547 1.173.547t1.167-.547q.428-.548.428-1.494 0-.947-.428-1.495-.429-.553-1.167-.553m0-.548q1.054 0 1.679.708.631.703.631 1.888 0 1.178-.631 1.887-.625.702-1.679.702t-1.685-.702q-.631-.703-.631-1.887t.631-1.888Q39.655.56 40.709.56\" class=\"atom\"/\u003e\u003cpath fill=\"#1ff01f\" stroke=\"none\" d=\"M42.727 46.763v.714q-.339-.321-.726-.476-.387-.161-.822-.161-.857 0-1.315.524-.453.524-.453 1.518 0 .988.453 1.512.458.524 1.315.524.435 0 .822-.155.387-.161.726-.476v.702q-.357.244-.756.363-.393.12-.833.12-1.137 0-1.792-.691-.649-.697-.649-1.899 0-1.209.649-1.899.655-.697 1.792-.697.446 0 .839.119.399.119.75.358m1.021-.596h.613v5.209h-.613z\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M65.209 15.892h.911l2.215 4.185v-4.185h.661v5.001h-.911l-2.221-4.185v4.185h-.655zM65.209 10.32h.679v2.048h2.459V10.32h.672v5.001h-.672V12.94h-2.459v2.381h-.679z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#1ff01f\" d=\"m37.311 46.916-4.899-2.828\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.824 20.286-4.96 2.864M70.387 20.289l4.957 2.862\" 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":"2-Chloromethcathinone","UNII":"843M5D2FGG","XLogP":2.1}