{"Abbreviation":["3,4-DMPIPPP"],"Aliases":["1-(3,4-Dihydroxyphenyl)-2-piperidin-1-ylpropan-1-one","Schembl10042343"],"ChemicalClasses":["cathinone","piperidinophenone"],"Chirality":"racemic","Erowid Experience Reports":[],"Esters":[],"Formating":["3,4-dihydroxy-alpha-piperidinopropiophenone"],"HeavyAtomCount":18,"IUPACName":"1-(3,4-dihydroxyphenyl)-2-piperidin-1-ylpropan-1-one","InChI":"InChI=1S/C14H19NO3/c1-10(15-7-3-2-4-8-15)14(18)11-5-6-12(16)13(17)9-11/h5-6,9-10,16-17H,2-4,7-8H2,1H3","InChIKey":"DIGTYXWSMJMTLM-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e14\u003c/sub\u003eH\u003csub\u003e19\u003c/sub\u003eNO\u003csub\u003e3\u003c/sub\u003e","MolecularWeight":"249.30 g/mol","PubChemId":214257,"PubChemTitle":"1-(3,4-Dihydroxyphenyl)-2-piperidin-1-ylpropan-1-one","Reddit Experience Reports":[],"RefCount":2,"RefCur":"","References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/214257","Name":"3,4-Dihydroxy-α-piperidinopropiophenone","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 214257, 3,4-Dihydroxy-α-piperidinopropiophenone. Accessed August 23, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/214257\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/214257\u003c/a\u003e"],"SMILES":"CC(C(=O)C1=CC(=C(C=C1)O)O)N2CCCCC2","SaltData":[],"Salts":[],"StereoisomerData":[{"ChemicalClasses":["cathinone","piperidinophenone"],"SMILES":"C[C@H](C(=O)C1=CC(O)=C(O)C=C1)N1CCCCC1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 113.958 57.608\"\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 0h114v58H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M73.652 31.595h-.801M73.985 34.135h-1.467M74.318 36.675h-2.133M74.652 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class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-3,4-Dihydroxy-α-piperidinopropiophenone"},{"ChemicalClasses":["cathinone","piperidinophenone"],"SMILES":"C[C@@H](C(=O)C1=CC(O)=C(O)C=C1)N1CCCCC1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 113.958 57.608\"\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 0h114v58H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M73.652 31.595h-.801l-2 15.24h4.801z\" class=\"bond\"/\u003e\u003cpath d=\"m73.252 31.595-13.199-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M58.834 24.679V12.928M61.273 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