{"Abbreviation":["3,4-DCPIPVP"],"Aliases":["1-(3,4-Dichlorophenyl)-2-piperidin-1-yl-pentan-1-one","Chembl204288","1-(3,4-dichlorophenyl)-2-piperidin-1-yl-pentan-1-one","Schembl4937310","Bdbm50182557","1-(3,4-Dichlorophenyl)-2-(1-piperidinyl)-1-pentanone"],"CAS":"850352-64-6","ChemicalClasses":["cathinone","piperidinophenone"],"Chirality":"racemic","DTXSID":"001342847","Erowid Experience Reports":[],"Esters":[],"Formating":["3',4'-dichloro-alpha-piperidinopentiophenone"],"HeavyAtomCount":20,"IUPACName":"1-(3,4-dichlorophenyl)-2-piperidin-1-ylpentan-1-one","InChI":"InChI=1S/C16H21Cl2NO/c1-2-6-15(19-9-4-3-5-10-19)16(20)12-7-8-13(17)14(18)11-12/h7-8,11,15H,2-6,9-10H2,1H3","InChIKey":"OVEGFFRUJIZDSI-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e16\u003c/sub\u003eH\u003csub\u003e21\u003c/sub\u003eCl\u003csub\u003e2\u003c/sub\u003eNO","MolecularWeight":"314.2 g/mol","PubChemId":11449834,"PubChemTitle":"1-(3,4-Dichlorophenyl)-2-piperidin-1-yl-pentan-1-one","Reddit Experience Reports":[],"RefCount":2,"RefCur":"","References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/11449834","Name":"3',4'-Dichloro-α-piperidinopentiophenone","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=850352-64-6","Name":"3',4'-Dichloro-α-piperidinopentiophenone","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID001342847","Name":"3',4'-Dichloro-α-piperidinopentiophenone","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 11449834, 3',4'-Dichloro-α-piperidinopentiophenone. Accessed August 23, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/11449834\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/11449834\u003c/a\u003e"],"SMILES":"CCCC(C(=O)C1=CC(=C(C=C1)Cl)Cl)N2CCCCC2","SaltData":[],"Salts":[],"StereoisomerData":[{"ChemicalClasses":["cathinone","piperidinophenone"],"SMILES":"CCC[C@H](C(=O)C1=CC(Cl)=C(Cl)C=C1)N1CCCCC1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 112.62 70.655\"\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=\"#1ff01f\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h113v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M85.113 69.695v-15.24M85.113 54.455l-13.199-7.62M71.914 46.835v-15.24M71.914 31.595l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M57.497 24.679V12.928M59.935 24.679V12.928\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M57.497 12.928v5.875M59.935 12.928v5.875\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m58.716 23.975-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m45.518 31.595-13.203-7.628M43.08 33.003l-10.766-6.221\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.315 23.967-13.198 7.62M19.117 31.587 7.61 24.945\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.117 31.587.004 15.248M21.555 32.994l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"M19.121 46.835 7.616 53.478M19.121 46.835l13.204 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m32.325 54.463 13.198-7.62M32.325 51.648l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m45.518 31.595.005 15.248\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m71.714 31.249.4.692M73.457 29.912l.686 1.188M75.199 28.576l.972 1.683M76.942 27.24l1.257 2.178M78.685 25.904l1.543 2.673M80.427 24.568l1.829 3.168\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m78.685 25.904.772 1.337M80.427 24.568l.914 1.584\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m85.111 19.874-.003-11.147M85.108 8.727l13.198-7.62M98.306 1.107l13.203 7.628M111.509 8.735l.005 15.248M111.514 23.983l-13.198 7.62M88.391 25.869l9.925 5.734\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M58.719 6.69q-.738 0-1.173.554-.428.547-.428 1.494t.428 1.494q.435.548 1.173.548t1.167-.548q.428-.547.428-1.494t-.428-1.494q-.429-.554-1.167-.554m0-.548q1.054 0 1.679.709.631.702.631 1.887 0 1.179-.631 1.887-.625.703-1.679.703t-1.685-.703-.631-1.887.631-1.887q.631-.709 1.685-.709\" class=\"atom\"/\u003e\u003cpath stroke=\"none\" d=\"M4.59 21.959v.715q-.339-.322-.726-.476-.387-.161-.822-.161-.857 0-1.315.524-.453.524-.453 1.518 0 .988.453 1.512.458.524 1.315.524.435 0 .822-.155.387-.161.726-.476v.702q-.357.244-.756.363-.393.119-.833.119-1.137 0-1.792-.69-.649-.697-.649-1.899 0-1.209.649-1.899.655-.697 1.792-.697.446 0 .839.119.399.119.75.357m1.02-.595h.614v5.209H5.61zM4.596 52.446v.714q-.339-.321-.726-.476-.387-.161-.821-.161-.858 0-1.316.524-.453.524-.453 1.518 0 .988.453 1.512.458.524 1.316.524.434 0 .821-.155.387-.16.726-.476v.703q-.357.244-.756.363-.393.119-.833.119-1.137 0-1.792-.691-.649-.696-.649-1.899 0-1.208.649-1.899.655-.696 1.792-.696.446 0 .839.119.399.119.75.357m1.021-.596h.613v5.209h-.613z\" class=\"atom\"/\u003e\u003cpath fill=\"#3050f8\" stroke=\"none\" d=\"M83.219 21.475h.911l2.215 4.185v-4.185h.661v5h-.911l-2.221-4.185v4.185h-.655z\" class=\"atom\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m7.61 24.945 5.754 3.321M7.616 53.478l5.752-3.321\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m85.111 19.874-.002-5.574M88.391 25.869l4.962 2.867\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-3',4'-Dichloro-α-piperidinopentiophenone"},{"ChemicalClasses":["cathinone","piperidinophenone"],"SMILES":"CCC[C@@H](C(=O)C1=CC(Cl)=C(Cl)C=C1)N1CCCCC1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 112.62 70.655\"\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=\"#1ff01f\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h113v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M85.113 69.695v-15.24M85.113 54.455l-13.199-7.62M71.914 46.835v-15.24M71.914 31.595l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M57.497 24.679V12.928M59.935 24.679V12.928\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M57.497 12.928v5.875M59.935 12.928v5.875\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m58.716 23.975-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m45.518 31.595-13.203-7.628M43.08 33.003l-10.766-6.221\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.315 23.967-13.198 7.62M19.117 31.587 7.61 24.945\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.117 31.587.004 15.248M21.555 32.994l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"M19.121 46.835 7.616 53.478M19.121 46.835l13.204 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m32.325 54.463 13.198-7.62M32.325 51.648l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m45.518 31.595.005 15.248\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m71.714 31.249.4.692 10.671-4.425-.951-1.648-.952-1.648z\" class=\"bond\"/\u003e\u003cpath d=\"m85.111 19.874-.003-11.147M85.108 8.727l13.198-7.62M98.306 1.107l13.203 7.628M111.509 8.735l.005 15.248M111.514 23.983l-13.198 7.62M88.391 25.869l9.925 5.734\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M58.719 6.69q-.738 0-1.173.554-.428.547-.428 1.494t.428 1.494q.435.548 1.173.548t1.167-.548q.428-.547.428-1.494t-.428-1.494q-.429-.554-1.167-.554m0-.548q1.054 0 1.679.709.631.702.631 1.887 0 1.179-.631 1.887-.625.703-1.679.703t-1.685-.703-.631-1.887.631-1.887q.631-.709 1.685-.709\" class=\"atom\"/\u003e\u003cpath stroke=\"none\" d=\"M4.59 21.959v.715q-.339-.322-.726-.476-.387-.161-.822-.161-.857 0-1.315.524-.453.524-.453 1.518 0 .988.453 1.512.458.524 1.315.524.435 0 .822-.155.387-.161.726-.476v.702q-.357.244-.756.363-.393.119-.833.119-1.137 0-1.792-.69-.649-.697-.649-1.899 0-1.209.649-1.899.655-.697 1.792-.697.446 0 .839.119.399.119.75.357m1.02-.595h.614v5.209H5.61zM4.596 52.446v.714q-.339-.321-.726-.476-.387-.161-.821-.161-.858 0-1.316.524-.453.524-.453 1.518 0 .988.453 1.512.458.524 1.316.524.434 0 .821-.155.387-.16.726-.476v.703q-.357.244-.756.363-.393.119-.833.119-1.137 0-1.792-.691-.649-.696-.649-1.899 0-1.208.649-1.899.655-.696 1.792-.696.446 0 .839.119.399.119.75.357m1.021-.596h.613v5.209h-.613z\" class=\"atom\"/\u003e\u003cpath fill=\"#3050f8\" stroke=\"none\" d=\"M83.219 21.475h.911l2.215 4.185v-4.185h.661v5h-.911l-2.221-4.185v4.185h-.655z\" class=\"atom\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m7.61 24.945 5.754 3.321M7.616 53.478l5.752-3.321\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m85.111 19.874-.002-5.574M88.391 25.869l4.962 2.867\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-3',4'-Dichloro-α-piperidinopentiophenone"}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-3',4'-Dichloro-α-piperidinopentiophenone","(S)-3',4'-Dichloro-α-piperidinopentiophenone"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 112.62 70.655\"\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=\"#1ff01f\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h113v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M85.113 69.695v-15.24M85.113 54.455l-13.199-7.62M71.914 46.835v-15.24M71.914 31.595l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M57.497 24.679V12.928M59.935 24.679V12.928\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M57.497 12.928v5.875M59.935 12.928v5.875\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m58.716 23.975-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m45.518 31.595-13.203-7.628M43.08 33.003l-10.766-6.221\"/\u003e\u003c/g\u003e\u003cpath d=\"m32.315 23.967-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.117 31.587.004 15.248M21.555 32.994l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m19.121 46.835 13.204 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m32.325 54.463 13.198-7.62M32.325 51.648l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m45.518 31.595.005 15.248M19.121 46.835 7.616 53.478M19.117 31.587 7.61 24.945M71.914 31.595l9.92-5.727M85.111 19.874l-.003-11.147M85.108 8.727l13.198-7.62M98.306 1.107l13.203 7.628M111.509 8.735l.005 15.248M111.514 23.983l-13.198 7.62M88.391 25.869l9.925 5.734\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M58.719 6.69q-.738 0-1.173.554-.428.547-.428 1.494t.428 1.494q.435.548 1.173.548t1.167-.548q.428-.547.428-1.494t-.428-1.494q-.429-.554-1.167-.554m0-.548q1.054 0 1.679.709.631.702.631 1.887 0 1.179-.631 1.887-.625.703-1.679.703t-1.685-.703-.631-1.887.631-1.887q.631-.709 1.685-.709\" class=\"atom\"/\u003e\u003cpath stroke=\"none\" d=\"M4.596 52.446v.714q-.339-.321-.726-.476-.387-.161-.821-.161-.858 0-1.316.524-.453.524-.453 1.518 0 .988.453 1.512.458.524 1.316.524.434 0 .821-.155.387-.16.726-.476v.703q-.357.244-.756.363-.393.119-.833.119-1.137 0-1.792-.691-.649-.696-.649-1.899 0-1.208.649-1.899.655-.696 1.792-.696.446 0 .839.119.399.119.75.357m1.021-.596h.613v5.209h-.613zM4.59 21.959v.715q-.339-.322-.726-.476-.387-.161-.822-.161-.857 0-1.315.524-.453.524-.453 1.518 0 .988.453 1.512.458.524 1.315.524.435 0 .822-.155.387-.161.726-.476v.702q-.357.244-.756.363-.393.119-.833.119-1.137 0-1.792-.69-.649-.697-.649-1.899 0-1.209.649-1.899.655-.697 1.792-.697.446 0 .839.119.399.119.75.357m1.02-.595h.614v5.209H5.61z\" class=\"atom\"/\u003e\u003cpath fill=\"#3050f8\" stroke=\"none\" d=\"M83.219 21.475h.911l2.215 4.185v-4.185h.661v5h-.911l-2.221-4.185v4.185h-.655z\" class=\"atom\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m7.616 53.478 5.752-3.321M7.61 24.945l5.754 3.321\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m81.834 25.868-4.96 2.863M85.111 19.874l-.002-5.574M88.391 25.869l4.962 2.867\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"3',4'-Dichloro-α-piperidinopentiophenone","XLogP":5.1}