{"Abbreviation":["2-MC"],"Aliases":["1198393-66-6","Schembl8391903","En300-1838619"],"ChemicalClasses":["cathinone"],"Chirality":"racemic","Erowid Experience Reports":[],"Esters":[],"Formating":[],"HeavyAtomCount":12,"IUPACName":"2-amino-1-(2-methylphenyl)propan-1-one","InChI":"InChI=1S/C10H13NO/c1-7-5-3-4-6-9(7)10(12)8(2)11/h3-6,8H,11H2,1-2H3","InChIKey":"UVUCPONHPJUZQN-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e10\u003c/sub\u003eH\u003csub\u003e13\u003c/sub\u003eNO","MolecularWeight":"163.22 g/mol","PubChemId":82415097,"RefCount":2,"RefCur":"","References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/82415097","Name":"2-Methylcathinone","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 82415097, 2-amino-1-(2-methylphenyl)propan-1-one. Accessed May 6, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/82415097\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/82415097\u003c/a\u003e"],"SMILES":"CC1=CC=CC=C1C(=O)C(C)N","SaltData":[],"Salts":[],"StereoisomerData":[{"ChemicalClasses":["cathinone"],"SMILES":"CC1=CC=CC=C1C(=O)[C@H](C)N","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 76.346 49.848\"\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=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h77v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m14.239 3.073-.003 15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.236 18.313-13.198 7.62M14.236 21.129 3.477 27.34\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.038 25.933.005 15.248\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.043 41.181 13.203 7.629M3.481 39.774l10.766 6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.246 48.81 13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.444 41.19-.004-15.249M25.006 39.782l-.004-12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 18.313 13.204 7.628M27.44 25.941l13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M39.419 19.025V7.002M41.857 19.025V7.002\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M39.419 7.002v6.011M41.857 7.002v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.638 18.321 13.198 7.62\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M54.186 25.941h-.7l-1.75 15.24h4.2z\" class=\"bond\"/\u003e\u003cpath d=\"m53.836 25.941 10.045-5.799\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M42.897 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T40.653.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 20.771h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578zM73.281 20.771h-.619v-2.286H70.15v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619zM75.786 22.26h-1.943v-.3l.771-.778q.222-.222.372-.393.153-.175.232-.34.079-.167.079-.364 0-.243-.147-.368-.143-.128-.371-.128-.215 0-.379.075-.161.075-.329.207l-.193-.243q.172-.147.393-.247.225-.1.508-.1.41 0 .65.208.239.207.239.575 0 .228-.096.432-.093.2-.265.396-.168.197-.393.418l-.614.604v.018h1.486z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.881 20.142-5.023 2.899\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-2-Methylcathinone"},{"ChemicalClasses":["cathinone"],"SMILES":"CC1=CC=CC=C1C(=O)[C@@H](C)N","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 76.346 49.848\"\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=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h77v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m14.239 3.073-.003 15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.236 18.313-13.198 7.62M14.236 21.129 3.477 27.34\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.038 25.933.005 15.248\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.043 41.181 13.203 7.629M3.481 39.774l10.766 6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.246 48.81 13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.444 41.19-.004-15.249M25.006 39.782l-.004-12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 18.313 13.204 7.628M27.44 25.941l13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M39.419 19.025V7.002M41.857 19.025V7.002\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M39.419 7.002v6.011M41.857 7.002v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.638 18.321 13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M54.186 25.941h-.7M54.478 28.481h-1.284M54.769 31.021h-1.866M55.061 33.561h-2.45M55.353 36.101h-3.034M55.645 38.641h-3.618M55.936 41.181h-4.2\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 25.941 10.045-5.799\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M42.897 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T40.653.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 20.771h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578zM73.281 20.771h-.619v-2.286H70.15v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619zM75.786 22.26h-1.943v-.3l.771-.778q.222-.222.372-.393.153-.175.232-.34.079-.167.079-.364 0-.243-.147-.368-.143-.128-.371-.128-.215 0-.379.075-.161.075-.329.207l-.193-.243q.172-.147.393-.247.225-.1.508-.1.41 0 .65.208.239.207.239.575 0 .228-.096.432-.093.2-.265.396-.168.197-.393.418l-.614.604v.018h1.486z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.881 20.142-5.023 2.899\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-2-Methylcathinone"}],"StereoisomerType":"enantiomer","Stereoisomers":["(S)-2-Methylcathinone","(R)-2-Methylcathinone"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 76.346 49.848\"\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=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h77v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m14.239 3.073-.003 15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.236 18.313-13.198 7.62M14.236 21.129 3.477 27.34\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.038 25.933.005 15.248\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.043 41.181 13.203 7.629M3.481 39.774l10.766 6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.246 48.81 13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.444 41.19-.004-15.249M25.006 39.782l-.004-12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 18.313 13.204 7.628M27.44 25.941l13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M39.419 19.025V7.002M41.857 19.025V7.002\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M39.419 7.002v6.011M41.857 7.002v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.638 18.321 13.198 7.62M53.836 25.941v15.24M53.836 25.941l10.045-5.799\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M42.897 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T40.653.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 20.771h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578zM73.281 20.771h-.619v-2.286H70.15v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619zM75.786 22.26h-1.943v-.3l.771-.778q.222-.222.372-.393.153-.175.232-.34.079-.167.079-.364 0-.243-.147-.368-.143-.128-.371-.128-.215 0-.379.075-.161.075-.329.207l-.193-.243q.172-.147.393-.247.225-.1.508-.1.41 0 .65.208.239.207.239.575 0 .228-.096.432-.093.2-.265.396-.168.197-.393.418l-.614.604v.018h1.486z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.881 20.142-5.023 2.899\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"2-Methylcathinone","XLogP":1.5}
