{"Abbreviation":["2-BZOPD"],"Aliases":["phenyl-piperidin-2-ylmethanone","Schembl1624945","Schembl5357416","Schembl8781912","Akos014195215"],"ChemicalClasses":["cathinone","2-benzylpiperidine"],"Chirality":"racemic","Erowid Experience Reports":[],"Esters":[],"Formating":[],"HeavyAtomCount":14,"IUPACName":"phenyl(piperidin-2-yl)methanone","InChI":"InChI=1S/C12H15NO/c14-12(10-6-2-1-3-7-10)11-8-4-5-9-13-11/h1-3,6-7,11,13H,4-5,8-9H2","InChIKey":"OXNQBVSEZJBIRI-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e12\u003c/sub\u003eH\u003csub\u003e15\u003c/sub\u003eNO","MolecularWeight":"189.25 g/mol","PubChemId":19772085,"RefCount":2,"RefCur":"","References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/19772085","Name":"2-Benzoylpiperidine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 19772085, phenyl(2-piperidinyl)methanone. Accessed May 8, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/19772085\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/19772085\u003c/a\u003e"],"SMILES":"C1CCNC(C1)C(=O)C2=CC=CC=C2","SaltData":[],"Salts":[],"StereoisomerData":[{"ChemicalClasses":["cathinone","2-benzylpiperidine"],"SMILES":"O=C(C1=CC=CC=C1)[C@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.246 49.818\"\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=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.617 18.313.002-11.31M38.179 16.905l.001-9.903\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m40.619 7.003-.001 5.655M38.18 7.002v4.952\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.617 18.313-13.192 7.614\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.425 25.927 14.23 18.3M24.987 27.334l-10.758-6.218\"/\u003e\u003c/g\u003e\u003cpath d=\"M14.23 18.3 1.038 25.914\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 25.914.003 15.24M3.477 27.322l.002 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 41.154 13.194 7.626\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.235 48.78 13.192-7.613M14.236 45.964l10.753-6.205\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.425 25.927.002 15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.632 26.234.35-.606M51.287 25.217l.642-1.112M48.943 24.2l.934-1.617M46.599 23.183l1.226-2.122M44.255 22.166l1.517-2.627M41.911 21.149l1.809-3.133M39.567 20.132l2.1-3.638\"/\u003e\u003c/g\u003e\u003cpath d=\"M53.807 25.931v15.231M53.807 41.162l13.2 7.616M67.007 48.778l13.201-7.616M80.208 41.162V25.931M80.208 25.931l-10.047-5.797M53.807 25.931l10.047-5.797\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M41.659 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T39.415.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.387 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.948 20.765h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.607 4.054h.03l-.018-.327q-.012-.22-.023-.476-.006-.262-.006-.483v-2.768h.577zM68.811 15.304h-.619v-2.286H65.68v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.161 20.134 5.023 2.898M70.161 20.134l5.023 2.898M63.854 20.134l-5.023 2.898M63.854 20.134l-5.023 2.898\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-2-Benzoylpiperidine"},{"ChemicalClasses":["cathinone","2-benzylpiperidine"],"SMILES":"O=C(C1=CC=CC=C1)[C@@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.246 49.818\"\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=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.617 18.313.002-11.31M38.179 16.905l.001-9.903\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m40.619 7.003-.001 5.655M38.18 7.002v4.952\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.617 18.313-13.192 7.614\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.425 25.927 14.23 18.3M24.987 27.334l-10.758-6.218\"/\u003e\u003c/g\u003e\u003cpath d=\"M14.23 18.3 1.038 25.914\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 25.914.003 15.24M3.477 27.322l.002 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 41.154 13.194 7.626\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.235 48.78 13.192-7.613M14.236 45.964l10.753-6.205\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.425 25.927.002 15.24\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m53.632 26.234.35-.606-13.365-9.913v2.598l-2.25 1.298z\" class=\"bond\"/\u003e\u003cpath d=\"M53.807 25.931v15.231M53.807 41.162l13.2 7.616M67.007 48.778l13.201-7.616M80.208 41.162V25.931M80.208 25.931l-10.047-5.797M53.807 25.931l10.047-5.797\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M41.659 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T39.415.56q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.387 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.948 20.765h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.607 4.054h.03l-.018-.327q-.012-.22-.023-.476-.006-.262-.006-.483v-2.768h.577zM68.811 15.304h-.619v-2.286H65.68v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.161 20.134 5.023 2.898M70.161 20.134l5.023 2.898M63.854 20.134l-5.023 2.898M63.854 20.134l-5.023 2.898\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-2-Benzoylpiperidine"}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-2-Benzoylpiperidine","(S)-2-Benzoylpiperidine"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.246 49.818\"\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=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m67.007 48.778 13.201-7.616M80.208 41.162V25.931M80.208 25.931l-10.047-5.797M63.854 20.134l-10.047 5.797M53.807 25.931v15.231M67.007 48.778l-13.2-7.616M53.807 25.931l-13.19-7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M39.398 19.016 39.4 7.002M41.836 19.017l.002-12.014\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m39.4 7.002-.001 6.007M41.838 7.003l-.001 6.007\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.617 18.313-13.192 7.613\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.425 25.926 14.23 18.3M24.987 27.334l-10.758-6.218\"/\u003e\u003c/g\u003e\u003cpath d=\"M14.23 18.3 1.038 25.914\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 25.914.003 15.24M3.477 27.322l.002 12.424\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 41.154 13.194 7.626\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.235 48.78 13.192-7.614M14.236 45.964l10.753-6.206\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.425 25.926.002 15.24\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.948 20.765h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.607 4.054h.03l-.018-.327q-.012-.221-.023-.477-.006-.261-.006-.482v-2.768h.577zM68.811 15.303h-.619v-2.286H65.68v2.286h-.613v-4.899h.613v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M42.879 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T40.634.56q.733 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.161 20.134 5.023 2.898M70.161 20.134l5.023 2.898M63.854 20.134l-5.023 2.898M63.854 20.134l-5.023 2.898\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"2-Benzoylpiperidine","XLogP":2.1}
