{"Abbreviation":["α-PIPPP"],"Aliases":["piperidino-propiophenone"],"ChemicalClasses":["piperidinophenone"],"Chirality":"racemic","Erowid Experience Reports":[],"Esters":[],"Formating":["alpha-piperidinopropiophenone"],"HeavyAtomCount":16,"IUPACName":"1-phenyl-2-piperidin-1-ylpropan-1-one","InChI":"InChI=1S/C14H19NO/c1-12(15-10-6-3-7-11-15)14(16)13-8-4-2-5-9-13/h2,4-5,8-9,12H,3,6-7,10-11H2,1H3","InChIKey":"GEHIWZFQDZBTBY-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e14\u003c/sub\u003eH\u003csub\u003e19\u003c/sub\u003eNO","MolecularWeight":"217.31 g/mol","PubChemId":458526,"RefCount":2,"RefCur":"","References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/458526","Name":"α-Piperidinopropiophenone","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 458526, α-Piperidinopropiophenone. Accessed August 7, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/458526\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/458526\u003c/a\u003e"],"SMILES":"CC(C(=O)C1=CC=CC=C1)N2CCCCC2","SaltData":[],"Salts":[],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"C[C@H](C(=O)C1=CC=CC=C1)N1CCCCC1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.474 55.433\"\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 0h95v56H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M54.186 31.527h-.7M54.478 34.067h-1.284M54.769 36.607h-1.866M55.061 39.147h-2.45M55.353 41.687h-3.034M55.645 44.227h-3.618M55.936 46.767h-4.2\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 31.527-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M39.419 24.611V12.588M41.857 24.611V12.588\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M39.419 12.588v6.011M41.857 12.588v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.638 23.907-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 31.527-13.204-7.629M25.002 32.934l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 23.898-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 31.518.005 15.249M3.477 32.926l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 46.767 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 54.395 13.198-7.62M14.247 51.579l10.759-6.211\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 31.527.004 15.248M53.836 31.527l10.045-5.8M70.187 25.728l10.05 5.807M80.237 31.535l13.199-7.62M93.436 23.915l-.005-15.248M93.431 8.667 80.228 1.038M80.228 1.038l-13.199 7.62M67.033 20.057l-.004-11.399\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M42.897 8.664q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .922.387 1.458.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.453\" class=\"atom\"/\u003e\u003cpath fill=\"#3050f8\" stroke=\"none\" d=\"M68.975 26.356h-.72l-2.62-4.066h-.03l.03.596q.024.357.024.732v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.327-.024-.477q-.006-.262-.006-.482v-2.768h.578z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.881 25.727-5.023 2.9M70.187 25.728l5.025 2.904M67.033 20.057l-.002-5.7\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-α-Piperidinopropiophenone","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"C[C@@H](C(=O)C1=CC=CC=C1)N1CCCCC1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.474 55.433\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h95v56H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath stroke=\"none\" d=\"M54.186 31.527h-.7l-1.75 15.24h4.2z\" class=\"bond\"/\u003e\u003cpath d=\"m53.836 31.527-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M39.419 24.611V12.588M41.857 24.611V12.588\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M39.419 12.588v6.011M41.857 12.588v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.638 23.907-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 31.527-13.204-7.629M25.002 32.934l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 23.898-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 31.518.005 15.249M3.477 32.926l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 46.767 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 54.395 13.198-7.62M14.247 51.579l10.759-6.211\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 31.527.004 15.248M53.836 31.527l10.045-5.8M70.187 25.728l10.05 5.807M80.237 31.535l13.199-7.62M93.436 23.915l-.005-15.248M93.431 8.667 80.228 1.038M80.228 1.038l-13.199 7.62M67.033 20.057l-.004-11.399\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M42.897 8.664q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .922.387 1.458.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.453\" class=\"atom\"/\u003e\u003cpath fill=\"#3050f8\" stroke=\"none\" d=\"M68.975 26.356h-.72l-2.62-4.066h-.03l.03.596q.024.357.024.732v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.327-.024-.477q-.006-.262-.006-.482v-2.768h.578z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.881 25.727-5.023 2.9M70.187 25.728l5.025 2.904M67.033 20.057l-.002-5.7\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-α-Piperidinopropiophenone","UNII":null}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-α-Piperidinopropiophenone","(S)-α-Piperidinopropiophenone"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.474 55.433\"\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 0h95v56H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M53.836 46.767v-15.24M53.836 31.527l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M39.419 24.611V12.588M41.857 24.611V12.588\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M39.419 12.588v6.011M41.857 12.588v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.638 23.907-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 31.527-13.204-7.629M25.002 32.934l-10.766-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 23.898-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 31.518.005 15.249M3.477 32.926l.004 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.043 46.767 13.203 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.246 54.395 13.198-7.62M14.247 51.579l10.759-6.211\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 31.527.004 15.248M53.836 31.527l10.045-5.8M70.187 25.728l10.05 5.807M80.237 31.535l13.199-7.62M93.436 23.915l-.005-15.248M93.431 8.667 80.228 1.038M80.228 1.038l-13.199 7.62M67.033 20.057l-.004-11.399\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M42.897 8.664q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .922.387 1.458.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.453\" class=\"atom\"/\u003e\u003cpath fill=\"#3050f8\" stroke=\"none\" d=\"M68.975 26.356h-.72l-2.62-4.066h-.03l.03.596q.024.357.024.732v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.327-.024-.477q-.006-.262-.006-.482v-2.768h.578z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m63.881 25.727-5.023 2.9M70.187 25.728l5.025 2.904M67.033 20.057l-.002-5.7\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"α-Piperidinopropiophenone","XLogP":2.9}