{"Aliases":["Dtxsid00274527","Dtxcid40226000","2-Amino-1,2-diphenylethan-1-one","desylamin","2-amino-1,2-diphenyl-ethanone","Acetophenone, 2-amino-2-phenyl-","2-Amino-2-phenylacetophenone","Schembl4919231","NSC126382","STL301398","Akos010297285","NSC-126382","CS-0289912","En300-146131"],"CAS":"3723-23-7","ChemicalClasses":["cathinone","1,2-diarylethylamine"],"Chirality":"racemic","Erowid Experience Reports":[],"Esters":[],"Formating":[],"HeavyAtomCount":16,"IUPACName":"2-amino-1,2-diphenylethanone","InChI":"InChI=1S/C14H13NO/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13H,15H2","InChIKey":"LKPGGRAYFGWREN-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e14\u003c/sub\u003eH\u003csub\u003e13\u003c/sub\u003eNO","MolecularWeight":"211.26 g/mol","PubChemId":13446,"RefChem":"336828","RefCount":2,"RefCur":"","References":[{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q82003889","Name":"Desylamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/13446","Name":"Desylamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=3723-23-7","Name":"Desylamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID00274527","Name":"Desylamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 13446, Desylamine. Accessed May 6, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/13446\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/13446\u003c/a\u003e"],"SMILES":"C1=CC=C(C=C1)C(C(=O)C2=CC=CC=C2)N","SaltData":[],"Salts":[],"StereoisomerData":[{"ChemicalClasses":["cathinone","1,2-diarylethylamine"],"SMILES":"N[C@@H](C(=O)C1=CC=CC=C1)C1=CC=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 76.346 72.699\"\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 0h77v73H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.661 25.638.35.606M55.715 24.115l.642 1.112M57.769 22.593l.933 1.617M59.823 21.07l1.225 2.122M61.876 19.548l1.517 2.627\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.393 22.175-.758-1.314\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 25.941-13.198-7.62\" 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=\"m27.44 25.941-13.204-7.628M25.002 27.349l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 18.313-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 25.933.005 15.248M3.477 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 48.81 13.198-7.62M14.247 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 25.941.004 15.249M53.836 25.941v15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m67.044 48.801-13.208-7.62M64.606 50.209l-10.77-6.213\"/\u003e\u003c/g\u003e\u003cpath d=\"M67.044 48.801v15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.836 71.661 13.208-7.62M53.836 68.846l10.77-6.213\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 71.661-13.208-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M40.628 48.801v15.24M43.066 50.209v12.424\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 41.181-13.208 7.62\" class=\"bond\"/\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 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\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-Desylamine"},{"ChemicalClasses":["cathinone","1,2-diarylethylamine"],"SMILES":"N[C@H](C(=O)C1=CC=CC=C1)C1=CC=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 76.346 72.699\"\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 0h77v73H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m53.661 25.638.35.606 10.711-4.646-.841-1.456-.841-1.457z\" class=\"bond\"/\u003e\u003cpath d=\"m53.836 25.941-13.198-7.62\" 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=\"m27.44 25.941-13.204-7.628M25.002 27.349l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 18.313-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 25.933.005 15.248M3.477 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 48.81 13.198-7.62M14.247 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 25.941.004 15.249M53.836 25.941v15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m67.044 48.801-13.208-7.62M64.606 50.209l-10.77-6.213\"/\u003e\u003c/g\u003e\u003cpath d=\"M67.044 48.801v15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.836 71.661 13.208-7.62M53.836 68.846l10.77-6.213\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 71.661-13.208-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M40.628 48.801v15.24M43.066 50.209v12.424\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 41.181-13.208 7.62\" class=\"bond\"/\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 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\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-Desylamine"}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-Desylamine","(S)-Desylamine"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 76.346 72.699\"\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 0h77v73H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.836 71.661 13.208-7.62M53.836 68.846l10.77-6.213\"/\u003e\u003c/g\u003e\u003cpath d=\"M67.044 64.041v-15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m67.044 48.801-13.208-7.62M64.606 50.209l-10.77-6.213\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 41.181-13.208 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M40.628 48.801v15.24M43.066 50.209v12.424\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 71.661-13.208-7.62M53.836 41.181v-15.24M53.836 25.941l-13.198-7.62\" 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=\"m27.44 25.941-13.204-7.628M25.002 27.349l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 18.313-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 25.933.005 15.248M3.477 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 48.81 13.198-7.62M14.247 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 25.941.004 15.249M53.836 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":"Desylamine","Wikidata":"Q82003889","XLogP":1.9}