{"Aliases":["Ritalinic acid","2-Phenyl-2-(piperidin-2-yl)acetic acid","α-Phenyl-2-piperidineacetic acid","Dtxsid20864888","Chebi:83481","2-Piperidineacetic acid, α-phenyl-","Dtxcid20813356","243-020-7","GT4165RS9H","Phenyl(2-piperidinyl)acetic acid","phenyl(piperidin-2-yl)acetic acid","2-Phenyl-2-(2-piperidyl)acetic Acid","α-Phenylpiperidine-2-acetic acid","Mfcd06200695","threo-Ritalinic acid","54631-24-2","threo-Ritalinic AcidSee R533110","2-Phenyl-2-piperidineacetic acid","Einecs 243-020-7","2-Phenyl-2-(2-piperidyl) acetic acid","Ritalinic acid, 99%","orb3029516","Schembl1462581","Ritalinic acid, analytical standard","MSK10554","Phenyl(2-piperidinyl)acetic acid #","I\u003c\u003c-Phenyl-2-piperidineacetic acid","s5251","2-Phenyl-2-(2-piperidy)acetic acid","α-Phenyl-2-piperidine acetic acid","Akos015892837","AC-8122","CS-W022954","FP33840","FS-3198","2-Phenyl-2-piperidineacetic acid, 98%","IR180350","Methylphenidate Hydrochloride Impurity 11","SY030346","DB-014888","Methylphenidate Hydrochloride EP Impurity A","NS00000318","R0111","(2RS)-phenyl[(2RS)-piperidin-2-yl]acetic acid","En300-7375458","F079084","Ritalinic Acid; Methylphenidate Related Compound A","Q17052328"],"CAS":"19395-41-6","ChemicalClasses":["phenidate"],"Chirality":"racemic","Erowid Experience Reports":[],"Esters":[],"European Community (EC) Number":"243-020-7","Formating":[],"HMDB ID":"HMDB0042008","HeavyAtomCount":16,"IUPACName":"2-phenyl-2-piperidin-2-ylacetic acid","InChI":"InChI=1S/C13H17NO2/c15-13(16)12(10-6-2-1-3-7-10)11-8-4-5-9-14-11/h1-3,6-7,11-12,14H,4-5,8-9H2,(H,15,16)","InChIKey":"INGSNVSERUZOAK-UHFFFAOYSA-N","MeSH Headers":[{"Id":"M0053672","Link":"https://id.nlm.nih.gov/mesh/M0053672.html","Name":"ritalinic acid","Ref":59},{"Id":"DescTree","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":"MeSH Tree","Ref":61},{"Id":"PubMed from MeSH","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":null,"Ref":73}],"MolecularFormula":"C\u003csub\u003e13\u003c/sub\u003eH\u003csub\u003e17\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"219.28 g/mol","PD":"PDK0106","PubChemId":86863,"RefChem":"883659","RefCount":2,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Ritalinic_acid","Name":"Ritalinic acid","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/86863","Name":"Ritalinic acid","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PDK0106","Name":"Ritalinic acid","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=19395-41-6","Name":"Ritalinic acid","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0042008","Name":"Ritalinic acid","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID20864888","Name":"Ritalinic acid","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 86863, Ritalinic acid. Accessed May 8, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/86863\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/86863\u003c/a\u003e"],"SMILES":"C1CCNC(C1)C(C2=CC=CC=C2)C(=O)O","SaltData":[],"Salts":[],"StereoisomerData":[{"SMILES":"O=C(O)[C@@H](C1=CC=CC=C1)[C@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 58.517\"\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 0h82v59H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.641 11.755 9.919-5.724M40.642 8.939l8.699-5.02\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M50.56 6.031 45.6 8.893M49.341 3.919l-4.349 2.51\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.641 11.755-9.921-5.73\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M40.289 26.995h.7M40.039 24.818h1.2M39.79 22.641h1.7M39.54 20.463l2.2.001M39.29 18.286l2.7.001M39.04 16.109l3.201.001M38.791 13.932h3.7M38.541 11.755h4.201\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.639 26.995-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.439 34.613-13.201-7.631M25.001 36.02l-10.764-6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"M14.238 26.982 1.038 34.6\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 34.6.003 15.249M3.477 36.008l.002 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 49.849 13.201 7.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 57.479 13.2-7.618M14.243 54.663l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 34.613.003 15.248M40.639 26.995l13.197 7.622M53.836 34.617v15.24M53.836 49.857l13.208 7.62M67.044 57.477l13.208-7.62M80.252 49.857v-15.24M80.252 34.617l-10.055-5.801\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.661 34.314.35.606M55.423 33.009l.6 1.039M57.185 31.704l.849 1.472M58.947 30.398l1.099 1.906M60.709 29.093l1.349 2.339M62.471 27.788l1.599 2.772\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m62.058 31.432-.675-1.17M64.07 30.56l-.8-1.386M62.471 27.788l.799 1.386\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M55.491 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-.881T53.246.56q.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\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M29.704 4.13q0 .756-.256 1.327-.256.566-.756.882-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.888-.244-.571-.244-1.333 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.233.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524T25.84 4.13M24.623 6.583h-.619V4.297h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V1.683h.619z\"/\u003e\u003c/g\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 29.447h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.482v-2.769h.578zM68.848 23.986h-.619V21.7h-2.513v2.286h-.613v-4.9h.613v2.072h2.513v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m30.72 6.025 4.96 2.865M30.72 6.025l4.96 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 28.816 5.028 2.9M70.197 28.816l5.028 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(4R,6S)-Ritalinic acid"},{"SMILES":"O=C(O)[C@@H](C1=CC=CC=C1)[C@@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 58.517\"\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 0h82v59H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.641 11.755 9.919-5.724M40.642 8.939l8.699-5.02\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M50.56 6.031 45.6 8.893M49.341 3.919l-4.349 2.51\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.641 11.755-9.921-5.73\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M40.289 26.995h.7M40.039 24.818h1.2M39.79 22.641h1.7M39.54 20.463l2.2.001M39.29 18.286l2.7.001M39.04 16.109l3.201.001M38.791 13.932h3.7M38.541 11.755h4.201\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.639 26.995-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.439 34.613-13.201-7.631M25.001 36.02l-10.764-6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"M14.238 26.982 1.038 34.6\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 34.6.003 15.249M3.477 36.008l.002 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 49.849 13.201 7.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 57.479 13.2-7.618M14.243 54.663l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 34.613.003 15.248M40.639 26.995l13.197 7.622M53.836 34.617v15.24M53.836 49.857l13.208 7.62M67.044 57.477l13.208-7.62M80.252 49.857v-15.24M80.252 34.617l-10.055-5.801\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m53.661 34.314.35.606 10.72-4.646-.841-1.458-.84-1.457z\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M55.491 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-.881T53.246.56q.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\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M29.704 4.13q0 .756-.256 1.327-.256.566-.756.882-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.888-.244-.571-.244-1.333 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.233.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524T25.84 4.13M24.623 6.583h-.619V4.297h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V1.683h.619z\"/\u003e\u003c/g\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 29.447h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.482v-2.769h.578zM68.848 23.986h-.619V21.7h-2.513v2.286h-.613v-4.9h.613v2.072h2.513v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m30.72 6.025 4.96 2.865M30.72 6.025l4.96 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 28.816 5.028 2.9M70.197 28.816l5.028 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(4S,6S)-Ritalinic acid"},{"SMILES":"O=C(O)[C@H](C1=CC=CC=C1)[C@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 58.517\"\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 0h82v59H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.641 11.755 9.919-5.724M40.642 8.939l8.699-5.02\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M50.56 6.031 45.6 8.893M49.341 3.919l-4.349 2.51\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.641 11.755-9.921-5.73\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M40.289 26.995h.7l1.902-16.538-2.25 1.298-2.249-1.299z\" class=\"bond\"/\u003e\u003cpath d=\"m40.639 26.995-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.439 34.613-13.201-7.631M25.001 36.02l-10.764-6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"M14.238 26.982 1.038 34.6\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 34.6.003 15.249M3.477 36.008l.002 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 49.849 13.201 7.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 57.479 13.2-7.618M14.243 54.663l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 34.613.003 15.248M40.639 26.995l13.197 7.622M53.836 34.617v15.24M53.836 49.857l13.208 7.62M67.044 57.477l13.208-7.62M80.252 49.857v-15.24M80.252 34.617l-10.055-5.801\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.661 34.314.35.606M55.423 33.009l.6 1.039M57.185 31.704l.849 1.472M58.947 30.398l1.099 1.906M60.709 29.093l1.349 2.339M62.471 27.788l1.599 2.772\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m62.058 31.432-.675-1.17M64.07 30.56l-.8-1.386M62.471 27.788l.799 1.386\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M55.491 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-.881T53.246.56q.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\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M29.704 4.13q0 .756-.256 1.327-.256.566-.756.882-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.888-.244-.571-.244-1.333 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.233.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524T25.84 4.13M24.623 6.583h-.619V4.297h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V1.683h.619z\"/\u003e\u003c/g\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 29.447h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.482v-2.769h.578zM68.848 23.986h-.619V21.7h-2.513v2.286h-.613v-4.9h.613v2.072h2.513v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m30.72 6.025 4.96 2.865M30.72 6.025l4.96 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 28.816 5.028 2.9M70.197 28.816l5.028 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(4R,6R)-Ritalinic acid"},{"SMILES":"O=C(O)[C@H](C1=CC=CC=C1)[C@@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 58.517\"\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 0h82v59H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.641 11.755 9.919-5.724M40.642 8.939l8.699-5.02\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M50.56 6.031 45.6 8.893M49.341 3.919l-4.349 2.51\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.641 11.755-9.921-5.73\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M40.289 26.995h.7l1.902-16.538-2.25 1.298-2.249-1.299z\" class=\"bond\"/\u003e\u003cpath d=\"m40.639 26.995-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.439 34.613-13.201-7.631M25.001 36.02l-10.764-6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"M14.238 26.982 1.038 34.6\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 34.6.003 15.249M3.477 36.008l.002 12.433\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 49.849 13.201 7.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 57.479 13.2-7.618M14.243 54.663l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 34.613.003 15.248M40.639 26.995l13.197 7.622M53.836 34.617v15.24M53.836 49.857l13.208 7.62M67.044 57.477l13.208-7.62M80.252 49.857v-15.24M80.252 34.617l-10.055-5.801\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m53.661 34.314.35.606 10.72-4.646-.841-1.458-.84-1.457z\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M55.491 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-.881T53.246.56q.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\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M29.704 4.13q0 .756-.256 1.327-.256.566-.756.882-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.888-.244-.571-.244-1.333 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.233.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524T25.84 4.13M24.623 6.583h-.619V4.297h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V1.683h.619z\"/\u003e\u003c/g\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 29.447h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.482v-2.769h.578zM68.848 23.986h-.619V21.7h-2.513v2.286h-.613v-4.9h.613v2.072h2.513v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m30.72 6.025 4.96 2.865M30.72 6.025l4.96 2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 28.816 5.028 2.9M70.197 28.816l5.028 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(4S,6R)-Ritalinic acid"}],"StereoisomerType":"diastereomer","Stereoisomers":["(4R,6S)-Ritalinic acid","(4S,6S)-Ritalinic acid","(4R,6R)-Ritalinic acid","(4S,6R)-Ritalinic acid"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 57.466\"\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 0h82v58H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m67.044 56.425 13.208-7.62M80.252 48.805v-15.24M80.252 33.565l-10.055-5.8M63.89 27.765l-10.054 5.8M53.836 33.565v15.24M67.044 56.425l-13.208-7.62M53.836 33.565l-13.197-7.622M40.639 25.943l-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.439 33.561-13.201-7.63M25.001 34.968l-10.764-6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.238 25.931-13.2 7.617\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 33.548.003 15.249M3.477 34.956l.002 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 48.797 13.201 7.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 56.427 13.2-7.617M14.243 53.612l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 33.561.003 15.249M40.639 25.943l.002-15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M39.422 9.999 49.95 3.923M40.641 12.111l10.528-6.076\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m49.95 3.923-5.264 3.038M51.169 6.035l-5.264 3.038\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.641 10.703-9.921-5.73\" class=\"bond\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 28.395h-.721l-2.619-4.066h-.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.578zM68.848 22.934h-.619v-2.286h-2.513v2.286h-.613v-4.899h.613v2.071h2.513v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M56.1 3.082q0 .756-.256 1.328-.256.565-.756.881t-1.244.316q-.756 0-1.262-.316t-.756-.887q-.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-3.864 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 stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M29.704 3.078q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T27.459.56q.732 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 1.452M24.623 5.531h-.619V3.245h-2.512v2.286h-.613v-4.9h.613v2.072h2.512V.631h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 27.765 5.028 2.9M70.197 27.765l5.028 2.9M63.89 27.765l-5.027 2.9M63.89 27.765l-5.027 2.9\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m30.72 4.973 4.96 2.865M30.72 4.973l4.96 2.865\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"Ritalinic acid","Wikipedia":"Ritalinic_acid","XLogP":-2.4}
