{"Abbreviation":"","Aliases":["acetylamphetamine","Acetamide, N-(1-methyl-2-phenylethyl)-","N-(1-Methyl-2-phenylethyl)acetamide","N-(α-Methylphenethyl)acetamide","Acetamide, N-(α-methylphenethyl)-","Acetamide, n-(α-methylphenethyl)-","Mls000532578","HMS2156K14","HMS3312M14","N-(α-methylphenethyl) acetamide","Ncgc00245536-01","N-(1-Phenylpropan-2-yl)ethanimidic acid","Smr000137517","CS-0235970","Ab00451056-08","En300-1659595"],"CAS":"14383-60-9","ChEBI":"CHEBI:191146","ChEMBL":"CHEMBL1588171","ChemicalClasses":["amphetamine"],"Chirality":"racemic","Classes":["Stimulant"],"Erowid Experience Reports":null,"Esters":[],"European Community (EC) Number":"111-691-4","Formating":[],"HeavyAtomCount":13,"IUPACName":"N-(1-phenylpropan-2-yl)acetamide","InChI":"InChI=1S/C11H15NO/c1-9(12-10(2)13)8-11-6-4-3-5-7-11/h3-7,9H,8H2,1-2H3,(H,12,13)","InChIKey":"YPKBVWZHVTZSPU-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e11\u003c/sub\u003eH\u003csub\u003e15\u003c/sub\u003eNO","MolecularWeight":"177.24 g/mol","PubChemId":26660,"RefCount":2,"RefCur":"","References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/26660","Name":"N-Acetylamphetamine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1588171","Name":"N-Acetylamphetamine","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:191146","Name":"N-Acetylamphetamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=14383-60-9","Name":"N-Acetylamphetamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID50932120","Name":"N-Acetylamphetamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 26660, N-Acetylamphetamine. Accessed July 19, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/26660\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/26660\u003c/a\u003e"],"SMILES":"CC(CC1=CC=CC=C1)NC(=O)C","SaltData":[],"Salts":[],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"CC(=O)N[C@H](C)Cc1ccccc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.469 39.997\"\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 0h95v40H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m93.431 8.471-13.199 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M81.452 15.387v12.022M79.013 15.387v12.022\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M81.452 27.409v-6.011M79.013 27.409v-6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m80.232 16.091-10.045-5.8M63.881 10.291l-10.045 5.8\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M54.186 16.091h-.7M54.436 18.268h-1.2M54.686 20.445h-1.7M54.936 22.622h-2.2M55.186 24.799h-2.7M55.436 26.977h-3.2M55.686 29.154h-3.7M55.936 31.331h-4.2\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 16.091-13.198-7.62M40.638 8.471l-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.44 16.091 14.236 8.462M25.002 17.498l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 8.462-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 16.082.005 15.249M3.477 17.49l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 31.331 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 38.959 13.198-7.62M14.247 36.143l10.759-6.211\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 16.091.004 15.248\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M82.492 31.328q0 .756-.256 1.327-.256.566-.756.881t-1.245.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.733 0 1.233.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 10.921h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483V6.021h.578zM68.838 5.459h-.619V3.173h-2.512v2.286h-.614V.56h.614v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.187 10.291 5.022 2.9M70.187 10.291l5.022 2.9M63.881 10.291l-5.023 2.9M63.881 10.291l-5.023 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-N-Acetylamphetamine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"CC(=O)N[C@@H](C)Cc1ccccc1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.469 39.997\"\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 0h95v40H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m93.431 8.471-13.199 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M81.452 15.387v12.022M79.013 15.387v12.022\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M81.452 27.409v-6.011M79.013 27.409v-6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m80.232 16.091-10.045-5.8M63.881 10.291l-10.045 5.8\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M54.186 16.091h-.7l-1.75 15.24h4.2z\" class=\"bond\"/\u003e\u003cpath d=\"m53.836 16.091-13.198-7.62M40.638 8.471l-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.44 16.091 14.236 8.462M25.002 17.498l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 8.462-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 16.082.005 15.249M3.477 17.49l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 31.331 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 38.959 13.198-7.62M14.247 36.143l10.759-6.211\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 16.091.004 15.248\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M82.492 31.328q0 .756-.256 1.327-.256.566-.756.881t-1.245.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.733 0 1.233.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 10.921h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483V6.021h.578zM68.838 5.459h-.619V3.173h-2.512v2.286h-.614V.56h.614v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.187 10.291 5.022 2.9M70.187 10.291l5.022 2.9M63.881 10.291l-5.023 2.9M63.881 10.291l-5.023 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-N-Acetylamphetamine","UNII":null}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-N-Acetylamphetamine","(S)-N-Acetylamphetamine"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.469 39.997\"\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 0h95v40H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M53.836 31.331v-15.24M53.836 16.091l-13.198-7.62M40.638 8.471l-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.44 16.091 14.236 8.462M25.002 17.498l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 8.462-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 16.082.005 15.249M3.477 17.49l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 31.331 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 38.959 13.198-7.62M14.247 36.143l10.759-6.211\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 16.091.004 15.248M53.836 16.091l10.045-5.8M70.187 10.291l10.045 5.8\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M81.452 15.387v12.022M79.013 15.387v12.022\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M81.452 27.409v-6.011M79.013 27.409v-6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m80.232 16.091 13.199-7.62\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.975 10.921h-.72l-2.62-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483V6.021h.578zM68.838 5.459h-.619V3.173h-2.512v2.286h-.614V.56h.614v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M82.492 31.328q0 .756-.256 1.327-.256.566-.756.881t-1.245.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.733 0 1.233.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.881 10.291-5.023 2.9M63.881 10.291l-5.023 2.9M70.187 10.291l5.022 2.9M70.187 10.291l5.022 2.9\" 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":"N-Acetylamphetamine","XLogP":1.9}
