{"Aliases":[],"ChemicalClasses":["phenylethylpyrrolidine"],"Chirality":"racemic","Erowid Experience Reports":[],"Esters":[],"Formating":[],"HeavyAtomCount":17,"IUPACName":"4-(2-pyrrolidin-1-ylpentyl)phenol","InChI":"InChI=1S/C15H23NO/c1-2-5-14(16-10-3-4-11-16)12-13-6-8-15(17)9-7-13/h6-9,14,17H,2-5,10-12H2,1H3","InChIKey":"NXCLNJZYQVSXTC-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e15\u003c/sub\u003eH\u003csub\u003e23\u003c/sub\u003eNO","MolecularWeight":"233.35 g/mol","PubChemId":101616944,"PubChemTitle":"4-(2-Pyrrolidin-1-ylpentyl)phenol","Reddit Experience Reports":[],"RefCount":2,"RefCur":"","References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/101616944","Name":"4-Hydroxyprolintane","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 101616944, 4-Hydroxyprolintane. Accessed August 23, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/101616944\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/101616944\u003c/a\u003e"],"SMILES":"CCCC(CC1=CC=C(C=C1)O)N2CCCC2","SaltData":[],"Salts":[],"StereoisomerData":[{"ChemicalClasses":["phenylethylpyrrolidine"],"SMILES":"CCC[C@H](CC1=CC=C(O)C=C1)N1CCCC1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 111.704 66.12\"\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 0h112v67H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M86.444 65.16V49.92M86.444 49.92 73.245 42.3M73.245 42.3V27.06M73.245 27.06l-13.198-7.62M60.047 19.44l-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m46.849 27.06-13.203-7.628M44.411 28.468l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m33.646 19.432-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m20.448 27.052.005 15.248M22.886 28.459l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m20.453 42.3-9.59 5.537M20.453 42.3l13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m33.656 49.929 13.198-7.62M33.656 47.113l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m46.849 27.06.005 15.249\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m73.045 26.714.4.693M75.078 25.155l.734 1.271M77.111 23.597l1.067 1.847M79.144 22.038l1.401 2.425M81.177 20.479l1.734 3.003\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m79.144 22.038.701 1.213M81.177 20.479l.867 1.501\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"M86.876 15.349 88.04 4.323M88.04 4.323l14.919-3.217M102.959 1.106l7.62 13.199M110.579 14.305l-10.246 11.312M89.799 20.932l10.534 4.685\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M7.257 47.875q-.738 0-1.173.554-.428.548-.428 1.494 0 .947.428 1.495.435.547 1.173.547t1.167-.547q.429-.548.429-1.495 0-.946-.429-1.494-.429-.554-1.167-.554m0-.547q1.054 0 1.679.708.631.703.631 1.887 0 1.179-.631 1.888-.625.702-1.679.702-1.053 0-1.684-.702-.632-.703-.632-1.888 0-1.184.632-1.887.631-.708 1.684-.708M.56 47.417h.679v2.048h2.458v-2.048h.673v5.001h-.673v-2.382H1.239v2.382H.56z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#3050f8\" stroke=\"none\" d=\"M84.551 16.94h.91l2.215 4.185V16.94h.661v5.001h-.911l-2.221-4.185v4.185h-.654z\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m10.863 47.837 4.795-2.768\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m86.876 15.349.582-5.513M89.799 20.932l5.267 2.342\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-4-Hydroxyprolintane"},{"ChemicalClasses":["phenylethylpyrrolidine"],"SMILES":"CCC[C@@H](CC1=CC=C(O)C=C1)N1CCCC1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 111.704 66.12\"\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 0h112v67H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M86.444 65.16V49.92M86.444 49.92 73.245 42.3M73.245 42.3V27.06M73.245 27.06l-13.198-7.62M60.047 19.44l-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m46.849 27.06-13.203-7.628M44.411 28.468l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m33.646 19.432-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m20.448 27.052.005 15.248M22.886 28.459l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m20.453 42.3-9.59 5.537M20.453 42.3l13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m33.656 49.929 13.198-7.62M33.656 47.113l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m46.849 27.06.005 15.249\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m73.045 26.714.4.693 10.671-4.425-.951-1.649-.952-1.648z\" class=\"bond\"/\u003e\u003cpath d=\"M86.876 15.349 88.04 4.323M88.04 4.323l14.919-3.217M102.959 1.106l7.62 13.199M110.579 14.305l-10.246 11.312M89.799 20.932l10.534 4.685\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M7.257 47.875q-.738 0-1.173.554-.428.548-.428 1.494 0 .947.428 1.495.435.547 1.173.547t1.167-.547q.429-.548.429-1.495 0-.946-.429-1.494-.429-.554-1.167-.554m0-.547q1.054 0 1.679.708.631.703.631 1.887 0 1.179-.631 1.888-.625.702-1.679.702-1.053 0-1.684-.702-.632-.703-.632-1.888 0-1.184.632-1.887.631-.708 1.684-.708M.56 47.417h.679v2.048h2.458v-2.048h.673v5.001h-.673v-2.382H1.239v2.382H.56z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#3050f8\" stroke=\"none\" d=\"M84.551 16.94h.91l2.215 4.185V16.94h.661v5.001h-.911l-2.221-4.185v4.185h-.654z\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m10.863 47.837 4.795-2.768\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m86.876 15.349.582-5.513M89.799 20.932l5.267 2.342\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-4-Hydroxyprolintane"}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-4-Hydroxyprolintane","(S)-4-Hydroxyprolintane"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 111.704 66.12\"\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 0h112v67H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M86.444 65.16V49.92M86.444 49.92 73.245 42.3M73.245 42.3V27.06M73.245 27.06l-13.198-7.62M60.047 19.44l-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m46.849 27.06-13.203-7.628M44.411 28.468l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m33.646 19.432-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m20.448 27.052.005 15.248M22.886 28.459l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m20.453 42.3 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m33.656 49.929 13.198-7.62M33.656 47.113l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m46.849 27.06.005 15.249M20.453 42.3l-9.59 5.537M73.245 27.06l9.92-5.727M86.876 15.349 88.04 4.323M88.04 4.323l14.919-3.217M102.959 1.106l7.62 13.199M110.579 14.305l-10.246 11.312M89.799 20.932l10.534 4.685\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M7.257 47.875q-.738 0-1.173.554-.428.548-.428 1.494 0 .947.428 1.495.435.547 1.173.547t1.167-.547q.429-.548.429-1.495 0-.946-.429-1.494-.429-.554-1.167-.554m0-.547q1.054 0 1.679.708.631.703.631 1.887 0 1.179-.631 1.888-.625.702-1.679.702-1.053 0-1.684-.702-.632-.703-.632-1.888 0-1.184.632-1.887.631-.708 1.684-.708M.56 47.417h.679v2.048h2.458v-2.048h.673v5.001h-.673v-2.382H1.239v2.382H.56z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#3050f8\" stroke=\"none\" d=\"M84.551 16.94h.91l2.215 4.185V16.94h.661v5.001h-.911l-2.221-4.185v4.185h-.654z\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m10.863 47.837 4.795-2.768\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m83.165 21.333-4.96 2.864M86.876 15.349l.582-5.513M89.799 20.932l5.267 2.342\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"4-Hydroxyprolintane","XLogP":3.7}