{"Abbreviation":["3-Me-MPH"],"Aliases":[],"ChemicalClasses":["phenidate"],"Chirality":"racemic","Classes":["Stimulant"],"Erowid Experience Reports":[],"Esters":[],"Formating":[],"HeavyAtomCount":18,"IUPACName":"methyl 2-(3-methylphenyl)-2-piperidin-2-ylacetate","InChI":"InChI=1S/C15H21NO2/c1-11-6-5-7-12(10-11)14(15(17)18-2)13-8-3-4-9-16-13/h5-7,10,13-14,16H,3-4,8-9H2,1-2H3","InChIKey":"NRBMYZAWNJOHPY-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e15\u003c/sub\u003eH\u003csub\u003e21\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"247.33 g/mol","PubChemId":56681582,"RefCount":2,"RefCur":"","References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/56681582","Name":"3-Methylmethylphenidate","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 56681582, Methyl 2-(3-methylphenyl)-2-piperidin-2-ylacetate. Accessed May 11, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/56681582\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/56681582\u003c/a\u003e"],"SMILES":"CC1=CC(=CC=C1)C(C2CCCCN2)C(=O)OC","SaltData":[],"Salts":[],"StereoisomerData":[{"SMILES":"COC(=O)[C@H](C1=CC=CC(C)=C1)[C@@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.488 70.535\"\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 0h95v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m40.645.91-.002 11.319M43.918 18.042l9.922 5.73\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.84 23.772 9.918-5.724M53.84 20.957l8.699-5.021\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m63.758 18.048-4.959 2.862M62.539 15.936l-4.349 2.511\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M53.487 39.012h.7l1.902-16.538-2.249 1.298-2.25-1.299z\" class=\"bond\"/\u003e\u003cpath d=\"M53.837 39.012 40.638 46.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.64 61.879-.002-15.249M38.202 60.471 38.2 48.037\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.64 61.879-13.199 7.617\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 61.866 13.202 7.63M16.677 60.459l10.765 6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.239 61.866-.003-15.249M14.236 46.617l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.436 39-13.2 7.617M27.435 41.815l-10.76 6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"M40.638 46.63 27.436 39M53.837 39.012l13.197 7.622M67.034 46.634v15.24M67.034 61.874l13.208 7.62M80.242 69.494l13.208-7.62M93.45 61.874v-15.24M93.45 46.634l-10.054-5.8\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"m66.859 46.331.35.607 10.72-4.647-.84-1.457-.841-1.458z\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M42.902 16.147q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.757-.887-.244-.572-.244-1.334 0-.75.244-1.309.251-.566.757-.882.506-.315 1.274-.315.732 0 1.232.315.5.31.756.876.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.529 1.221.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452M68.689 15.095q0 .756-.256 1.328-.256.565-.756.881t-1.244.316q-.756 0-1.262-.316t-.756-.887q-.245-.572-.245-1.334 0-.75.245-1.309.25-.566.756-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.452\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M82.183 41.464h-.72l-2.62-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM82.046 36.003h-.619v-2.286h-2.512v2.286h-.614v-4.899h.614v2.071h2.512v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m40.643 12.229.001-5.66M43.918 18.042l4.961 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m83.396 40.834 5.027 2.9M83.396 40.834l5.027 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(7R,8S)-3-Methylmethylphenidate"},{"SMILES":"COC(=O)[C@@H](C1=CC=CC(C)=C1)[C@@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.488 70.535\"\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 0h95v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m40.645.91-.002 11.319M43.918 18.042l9.922 5.73\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.84 23.772 9.918-5.724M53.84 20.957l8.699-5.021\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m63.758 18.048-4.959 2.862M62.539 15.936l-4.349 2.511\" class=\"hi\"/\u003e\u003c/g\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M53.487 39.012h.7M53.237 36.835h1.201M52.988 34.658h1.7M52.738 32.481h2.2M52.488 30.303l2.701.001M52.239 28.126l3.2.001M51.989 25.949l3.701.001M51.739 23.772l4.201.001\"/\u003e\u003c/g\u003e\u003cpath d=\"M53.837 39.012 40.638 46.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.64 61.879-.002-15.249M38.202 60.471 38.2 48.037\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.64 61.879-13.199 7.617\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 61.866 13.202 7.63M16.677 60.459l10.765 6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.239 61.866-.003-15.249M14.236 46.617l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.436 39-13.2 7.617M27.435 41.815l-10.76 6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"M40.638 46.63 27.436 39M53.837 39.012l13.197 7.622M67.034 46.634v15.24M67.034 61.874l13.208 7.62M80.242 69.494l13.208-7.62M93.45 61.874v-15.24M93.45 46.634l-10.054-5.8\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m66.859 46.331.35.607 10.72-4.647-.84-1.457-.841-1.458z\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M42.902 16.147q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.757-.887-.244-.572-.244-1.334 0-.75.244-1.309.251-.566.757-.882.506-.315 1.274-.315.732 0 1.232.315.5.31.756.876.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.529 1.221.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452M68.689 15.095q0 .756-.256 1.328-.256.565-.756.881t-1.244.316q-.756 0-1.262-.316t-.756-.887q-.245-.572-.245-1.334 0-.75.245-1.309.25-.566.756-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.452\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M82.183 41.464h-.72l-2.62-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM82.046 36.003h-.619v-2.286h-2.512v2.286h-.614v-4.899h.614v2.071h2.512v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m40.643 12.229.001-5.66M43.918 18.042l4.961 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m83.396 40.834 5.027 2.9M83.396 40.834l5.027 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(7S,8S)-3-Methylmethylphenidate"},{"SMILES":"COC(=O)[C@H](C1=CC=CC(C)=C1)[C@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.488 70.535\"\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 0h95v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m40.645.91-.002 11.319M43.918 18.042l9.922 5.73\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.84 23.772 9.918-5.724M53.84 20.957l8.699-5.021\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m63.758 18.048-4.959 2.862M62.539 15.936l-4.349 2.511\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M53.487 39.012h.7l1.902-16.538-2.249 1.298-2.25-1.299z\" class=\"bond\"/\u003e\u003cpath d=\"M53.837 39.012 40.638 46.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.64 61.879-.002-15.249M38.202 60.471 38.2 48.037\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.64 61.879-13.199 7.617\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 61.866 13.202 7.63M16.677 60.459l10.765 6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.239 61.866-.003-15.249M14.236 46.617l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.436 39-13.2 7.617M27.435 41.815l-10.76 6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"M40.638 46.63 27.436 39M53.837 39.012l13.197 7.622M67.034 46.634v15.24M67.034 61.874l13.208 7.62M80.242 69.494l13.208-7.62M93.45 61.874v-15.24M93.45 46.634l-10.054-5.8\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m66.859 46.331.35.607M68.621 45.026l.6 1.04M70.383 43.721l.85 1.473M72.145 42.416l1.1 1.906M73.907 41.111l1.349 2.339M75.669 39.805l1.599 2.773\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m75.256 43.45-.674-1.169M77.268 42.578l-.799-1.386M75.669 39.805l.8 1.387\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M42.902 16.147q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.757-.887-.244-.572-.244-1.334 0-.75.244-1.309.251-.566.757-.882.506-.315 1.274-.315.732 0 1.232.315.5.31.756.876.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.529 1.221.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452M68.689 15.095q0 .756-.256 1.328-.256.565-.756.881t-1.244.316q-.756 0-1.262-.316t-.756-.887q-.245-.572-.245-1.334 0-.75.245-1.309.25-.566.756-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.452\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M82.183 41.464h-.72l-2.62-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM82.046 36.003h-.619v-2.286h-2.512v2.286h-.614v-4.899h.614v2.071h2.512v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m40.643 12.229.001-5.66M43.918 18.042l4.961 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m83.396 40.834 5.027 2.9M83.396 40.834l5.027 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(7R,8R)-3-Methylmethylphenidate"},{"SMILES":"COC(=O)[C@@H](C1=CC=CC(C)=C1)[C@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.488 70.535\"\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 0h95v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m40.645.91-.002 11.319M43.918 18.042l9.922 5.73\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.84 23.772 9.918-5.724M53.84 20.957l8.699-5.021\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m63.758 18.048-4.959 2.862M62.539 15.936l-4.349 2.511\" class=\"hi\"/\u003e\u003c/g\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M53.487 39.012h.7M53.237 36.835h1.201M52.988 34.658h1.7M52.738 32.481h2.2M52.488 30.303l2.701.001M52.239 28.126l3.2.001M51.989 25.949l3.701.001M51.739 23.772l4.201.001\"/\u003e\u003c/g\u003e\u003cpath d=\"M53.837 39.012 40.638 46.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.64 61.879-.002-15.249M38.202 60.471 38.2 48.037\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.64 61.879-13.199 7.617\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 61.866 13.202 7.63M16.677 60.459l10.765 6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.239 61.866-.003-15.249M14.236 46.617l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.436 39-13.2 7.617M27.435 41.815l-10.76 6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"M40.638 46.63 27.436 39M53.837 39.012l13.197 7.622M67.034 46.634v15.24M67.034 61.874l13.208 7.62M80.242 69.494l13.208-7.62M93.45 61.874v-15.24M93.45 46.634l-10.054-5.8\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m66.859 46.331.35.607M68.621 45.026l.6 1.04M70.383 43.721l.85 1.473M72.145 42.416l1.1 1.906M73.907 41.111l1.349 2.339M75.669 39.805l1.599 2.773\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m75.256 43.45-.674-1.169M77.268 42.578l-.799-1.386M75.669 39.805l.8 1.387\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M42.902 16.147q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.757-.887-.244-.572-.244-1.334 0-.75.244-1.309.251-.566.757-.882.506-.315 1.274-.315.732 0 1.232.315.5.31.756.876.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.529 1.221.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452M68.689 15.095q0 .756-.256 1.328-.256.565-.756.881t-1.244.316q-.756 0-1.262-.316t-.756-.887q-.245-.572-.245-1.334 0-.75.245-1.309.25-.566.756-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.452\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M82.183 41.464h-.72l-2.62-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM82.046 36.003h-.619v-2.286h-2.512v2.286h-.614v-4.899h.614v2.071h2.512v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m40.643 12.229.001-5.66M43.918 18.042l4.961 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m83.396 40.834 5.027 2.9M83.396 40.834l5.027 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(7S,8R)-3-Methylmethylphenidate"}],"StereoisomerType":"diastereomer","Stereoisomers":["(7R,8S)-3-Methylmethylphenidate","(7S,8S)-3-Methylmethylphenidate","(7R,8R)-3-Methylmethylphenidate","(7S,8R)-3-Methylmethylphenidate"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 94.488 70.535\"\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 0h95v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m1.038 38.997 13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.436 39-13.2 7.617M27.435 41.815l-10.76 6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.436 39 13.202 7.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.64 61.879-.002-15.249M38.202 60.471 38.2 48.037\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.64 61.879-13.199 7.617\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.239 61.866 13.202 7.63M16.677 60.459l10.765 6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.236 46.617.003 15.249M40.638 46.63l13.199-7.618M53.837 39.012l13.197 7.622M67.034 46.634v15.24M67.034 61.874l13.208 7.62M80.242 69.494l13.208-7.62M93.45 61.874v-15.24M93.45 46.634l-10.054-5.8M67.034 46.634l10.055-5.8M53.837 39.012l.003-15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m52.621 23.068 10.527-6.076M53.839 25.18l10.528-6.076\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m63.148 16.992-5.263 3.038M64.367 19.104l-5.264 3.038\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.84 23.772-9.922-5.73M40.643 12.229 40.645.91\" class=\"bond\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M82.183 41.464h-.72l-2.62-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM82.046 36.003h-.619v-2.286h-2.512v2.286h-.614v-4.899h.614v2.071h2.512v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M69.298 16.151q0 .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-.881t1.274-.316q.732 0 1.232.316.5.309.756.875.256.565.256 1.327m-3.863 0q0 .923.387 1.459.393.53 1.22.53.839 0 1.22-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.208-.524-.833 0-1.226.524t-.393 1.452M42.902 16.147q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.757-.887-.244-.572-.244-1.334 0-.75.244-1.309.251-.566.757-.882.506-.315 1.274-.315.732 0 1.232.315.5.31.756.876.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.529 1.221.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.208-.524-.834 0-1.227.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m83.396 40.834 5.027 2.9M83.396 40.834l5.027 2.9M77.089 40.834l-5.028 2.9M77.089 40.834l-5.028 2.9\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m43.918 18.042 4.961 2.865M40.643 12.229l.001-5.66\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Subjective Effects":{"Cognitive Effects":["Analysis enhancement","Ego inflation","Focus enhancement","Increased music appreciation","Motivation enhancement","Thought acceleration","Wakefulness","Disinhibition","Suggestibility suppression","Cognitive euphoria","Compulsive redosing","Mania"],"Physical Effects":["Increased libido","Stamina enhancement","Stimulation","Appetite suppression","Dehydration","Dry mouth","Restless legs","Shakiness","Teeth grinding","Abnormal heartbeat","Increased blood pressure","Increased heart rate","Vasoconstriction"],"Visual Effects":[]},"Title":"3-Methylmethylphenidate","XLogP":0.6}
