{"Abbreviation":["MXiPr"],"Aliases":["2-(Isopropylamino)-2-(3-methoxyphenyl)cyclohexanone","2-(3-Methoxyphenyl)-2-((propan-2-yl)amino)cyclohexan-1-one","RefChem:157046"],"ChemicalClasses":["arylcyclohexylamine"],"Chirality":"racemic","Esters":[],"Formating":[],"HeavyAtomCount":19,"IUPACName":"2-(3-methoxyphenyl)-2-(propan-2-ylamino)cyclohexan-1-one","InChI":"InChI=1S/C16H23NO2/c1-12(2)17-16(10-5-4-9-15(16)18)13-7-6-8-14(11-13)19-3/h6-8,11-12,17H,4-5,9-10H2,1-3H3","InChIKey":"FTQIVDGNGXPEKP-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e16\u003c/sub\u003eH\u003csub\u003e23\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"261.36 g/mol","Opticalactivity":"( + / - )","PubChemId":163192824,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Methoxisopropamine","Name":"Methoxisopropamine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q107177557","Name":"Methoxisopropamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/163192824","Name":"Methoxisopropamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/KHM3GXB3S9","Name":"Methoxisopropamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID101336877","Name":"Methoxisopropamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 163192824, Methoxisopropamine. Accessed September 7, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/163192824\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/163192824\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Methoxisopropamine. UNII: KHM3GXB3S9. Global Substance Registration System. Accessed September 7, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/KHM3GXB3S9\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/KHM3GXB3S9\u003c/a\u003e"],"SMILES":"CC(C)NC1(CCCCC1=O)C2=CC(=CC=C2)OC","SaltData":[],"Salts":[],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"COC1=CC=CC([C@]2(NC(C)C)CCCCC2=O)=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 76.037 96.244\"\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=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h77v97H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m16.544 1.053 7.266 8.623M25.006 16.465l-3.825 10.574\" class=\"bond\"/\u003e\u003cg 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class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-Methoxisopropamine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"COC1=CC=CC([C@@]2(NC(C)C)CCCCC2=O)=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 76.037 96.244\"\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=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h77v97H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m16.544 1.053 7.266 8.623M25.006 16.465l-3.825 10.574\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M21.181 27.039 6.26 29.723M20.223 29.689 8.072 31.874\"/\u003e\u003c/g\u003e\u003cpath d=\"M6.26 29.723 1.053 44.045\" class=\"bond\"/\u003e\u003cg 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