{"Abbreviation":["N-pyrrolidinyl-3,4-DMA"],"Aliases":["N-pyrrolidinyl-3,4-DMA","Schembl10411188"],"ChemicalClasses":["phenylethylpyrrolidine"],"Chirality":"racemic","DTXSID":"001342354","Erowid Experience Reports":[],"Esters":[],"Formating":[],"HeavyAtomCount":18,"IUPACName":"1-[1-(3,4-dimethoxyphenyl)propan-2-yl]pyrrolidine","InChI":"InChI=1S/C15H23NO2/c1-12(16-8-4-5-9-16)10-13-6-7-14(17-2)15(11-13)18-3/h6-7,11-12H,4-5,8-10H2,1-3H3","InChIKey":"JFBIKRRRXMPOJC-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e15\u003c/sub\u003eH\u003csub\u003e23\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"249.35 g/mol","PubChemId":14879074,"PubChemTitle":"N-pyrrolidinyl-3,4-DMA","Reddit Experience Reports":[],"RefCount":2,"RefCur":"","References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/14879074","Name":"N-Pyrrolidinyl-3,4-dimethoxyamphetamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID001342354","Name":"N-Pyrrolidinyl-3,4-dimethoxyamphetamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 14879074, N-Pyrrolidinyl-3,4-dimethoxyamphetamine. Accessed August 23, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/14879074\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/14879074\u003c/a\u003e"],"SMILES":"CC(CC1=CC(=C(C=C1)OC)OC)N2CCCC2","SaltData":[],"Salts":[],"StereoisomerData":[{"ChemicalClasses":["phenylethylpyrrolidine"],"SMILES":"COC1=C(OC)C=C(C[C@@H](C)N2CCCC2)C=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 118.759 53.073\"\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=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h119v54H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m1.111 42.3 9.591 5.537M17.918 47.837l9.59-5.537\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath 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class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M14.313 47.875q-.739 0-1.173.554-.429.548-.429 1.494 0 .947.429 1.495.434.547 1.173.547.738 0 1.166-.547.429-.548.429-1.495 0-.946-.429-1.494-.428-.554-1.166-.554m0-.547q1.053 0 1.678.708.631.703.631 1.887 0 1.179-.631 1.888-.625.702-1.678.702-1.054 0-1.685-.702-.631-.703-.631-1.888 0-1.184.631-1.887.631-.708 1.685-.708M14.306 17.389q-.738 0-1.172.554-.429.547-.429 1.494t.429 1.494q.434.548 1.172.548.739 0 1.167-.548.429-.547.429-1.494t-.429-1.494q-.428-.554-1.167-.554m0-.548q1.054 0 1.679.709.631.702.631 1.887 0 1.179-.631 1.887-.625.703-1.679.703-1.053 0-1.684-.703-.631-.702-.631-1.887t.631-1.887q.631-.709 1.684-.709\" class=\"atom\"/\u003e\u003cpath fill=\"#3050f8\" stroke=\"none\" d=\"M91.606 16.94h.911l2.214 4.185V16.94h.661v5.001h-.911l-2.22-4.185v4.185h-.655z\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m10.702 47.837-4.795-2.768M17.918 47.837l4.795-2.768M17.912 21.517l4.795 2.768M10.693 21.52 5.9 24.288\" 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