{"Abbreviation":["RTI-121"],"CAS":"146145-21-3","ChemicalClasses":["phenyltropane"],"Chirality":"achiral","Classes":["Stimulant"],"EliminationHalfLife":"","Esters":[],"Formating":["2beta-carboisopropoxy-3beta-(4-iodophenyl)tropane"],"HeavyAtomCount":22,"IUPACName":"propan-2-yl (1R,2S,3S)-3-(4-iodophenyl)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylate","InChI":"InChI=1S/C18H24INO2/c1-11(2)22-18(21)17-15(12-4-6-13(19)7-5-12)10-14-8-9-16(17)20(14)3/h4-7,11,14-17H,8-10H2,1-3H3/t14?,15-,16-,17+/m1/s1","InChIKey":"ZAQLTGAFVMGUMB-IFFAKLHKSA-N","MolecularFormula":"C\u003csub\u003e18\u003c/sub\u003eH\u003csub\u003e24\u003c/sub\u003eINO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"413.3 g/mol","PubChemId":122190,"RefCount":2,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/RTI-121","Name":"2β-Carboisopropoxy-3β-(4-iodophenyl)tropane","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q7277828","Name":"2β-Carboisopropoxy-3β-(4-iodophenyl)tropane","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/122190","Name":"2β-Carboisopropoxy-3β-(4-iodophenyl)tropane","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=146145-21-3","Name":"2β-Carboisopropoxy-3β-(4-iodophenyl)tropane","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID70912323","Name":"2β-Carboisopropoxy-3β-(4-iodophenyl)tropane","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 122190, 3beta-(4-Iodophenyl)tropan-2beta-carboxylic acid isopropyl ester. Accessed November 11, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/122190\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/122190\u003c/a\u003e"],"SMILES":"CC(C)OC(=O)[C@@H]1[C@H]2CCC(N2C)C[C@@H]1C3=CC=C(C=C3)I","SaltData":[],"Salts":[],"Scheduling":[],"StereoisomerData":[],"Stereoisomers":[],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 85.164 114.969\"\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 0h86v115H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m1.014 62.758 14.181-5.582M15.195 57.176l2.256-15.072M15.195 57.176l8.905 7.087M30.634 65.283 41.3 61.084\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m41.3 61.084 1.672-11.166M39.097 59.331l1.463-9.774\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m42.972 49.918-.836 5.583M40.56 49.557l-.731 4.887\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"m53.007 70.848.436-.548-11.758-11.785-.385 2.569-2.416.951z\" class=\"bond\"/\u003e\u003cpath d=\"m53.225 70.574-3.353 14.833M49.872 85.407l9.449 11.888\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M59.321 97.645a.376.376 0 0 1-.35-.35c0-.176.175-.351.35-.351h6.487v.701zm8.419 0v-.701h6.825q.051-.048.099-.047c.137 0 .251.256.251.398 0 .175-.175.35-.35.35z\" class=\"bond\"/\u003e\u003cpath d=\"m74.561 97.295 9.551-11.888M84.112 85.407 70.15 88.364\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"m49.946 85.065-.147.684 13.36 4.322.371-1.72.371-1.719z\" class=\"bond\"/\u003e\u003cpath d=\"m66.833 92.915-.039 21.143M84.112 85.407l-3.455-14.833M80.657 70.574 66.941 63.97M53.225 70.574l13.716-6.604\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M66.591 63.97h.7l1.899-16.538-2.249 1.298-2.249-1.298z\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.733 41.11 13.208 7.62M56.172 39.701l10.769 6.214\"/\u003e\u003c/g\u003e\u003cpath d=\"M53.733 41.11V25.87\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m66.941 18.25-13.208 7.62M66.941 21.065l-10.769 6.213\"/\u003e\u003c/g\u003e\u003cpath d=\"m66.941 18.25 13.208 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M80.149 41.11V25.87M77.711 39.701V27.278\"/\u003e\u003c/g\u003e\u003cpath d=\"m66.941 48.73 13.208-7.62M66.941 18.25V6.86\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M29.379 66.663q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.757 0-1.263-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.733 0 1.233.315.5.31.756.876.256.565.256 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-.524-1.209-.524-.833 0-1.226.524-.393.523-.393 1.452M44.61 45.828q0 .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-3.864 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\u003cpath fill=\"#3050f8\" stroke=\"none\" d=\"M68.78 91.515h-.72l-2.619-4.066h-.03l.03.595q.023.357.023.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.017-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577z\" class=\"atom\"/\u003e\u003cpath fill=\"#940094\" stroke=\"none\" d=\"M67.825 5.459h-1.768v-.357l.578-.131V1.054l-.578-.137V.56h1.768v.357l-.571.137v3.917l.571.131z\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m24.1 64.263-4.452-3.543M30.634 65.283l5.333-2.099\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.15 88.364 6.981-1.478M66.833 92.915l-.019 10.572\" class=\"hi\"/\u003e\u003cpath stroke=\"#940094\" d=\"M66.941 6.86v5.695\" 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":"2β-Carboisopropoxy-3β-(4-iodophenyl)tropane","Wikidata":"Q7277828","Wikipedia":"RTI-121","XLogP":4.1}