{"Abbreviation":["4-FPM","4F-Phenmetrazine","PAL-748"],"Aliases":["4-Fpm","PAL-748","3-Methyl-(4-fluoro-2-phenyl)morpholine","Morpholine, 2-(4-fluorophenyl)-3-methyl-","Unii-aeu8y7h4q6","Schembl2599478","Dtxsid701341957"],"CAS":"1097796-73-0","ChemicalClasses":["2-phenylmorpholine"],"Chirality":"racemic","Erowid Experience Reports":[],"Esters":[],"Formating":[],"HeavyAtomCount":14,"IUPACName":"2-(4-fluorophenyl)-3-methylmorpholine","InChI":"InChI=1S/C11H14FNO/c1-8-11(14-7-6-13-8)9-2-4-10(12)5-3-9/h2-5,8,11,13H,6-7H2,1H3","InChIKey":"CLXPYTBRAZHUFD-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e11\u003c/sub\u003eH\u003csub\u003e14\u003c/sub\u003eFNO","MolecularWeight":"195.23 g/mol","PubChemId":43350789,"RefChem":"99037","RefCount":2,"RefCur":"","References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/43350789","Name":"4-Fluorophenmetrazine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=1097796-73-0","Name":"4-Fluorophenmetrazine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/AEU8Y7H4Q6","Name":"4-Fluorophenmetrazine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID701341957","Name":"4-Fluorophenmetrazine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 43350789, 4-Fluorophenmetrazine. Accessed May 12, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/43350789\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/43350789\u003c/a\u003e"],"SMILES":"CC1C(OCCN1)C2=CC=C(C=C2)F","SaltData":[],"Salts":[],"StereoisomerData":[{"SMILES":"C[C@H]1NCCO[C@@H]1C1=CC=C(F)C=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 87.888 57.367\"\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 0h88v58H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M68.236 31.518h-.7M68.528 34.057h-1.284M68.82 36.595l-1.867.001M69.112 39.134h-2.45M69.404 41.672l-3.034.001M69.696 44.211h-3.617M69.988 46.749l-4.2.001\"/\u003e\u003c/g\u003e\u003cpath d=\"m67.886 31.518 10.042-5.802M81.083 20.044l.003-11.39M81.086 8.654 67.895 1.038M67.895 1.038l-9.918 5.731M54.698 12.584l-.003 11.318M67.886 31.518l-13.191-7.616\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m54.87 24.206-.35-.607-15.266 6.618 2.249 1.299v2.597z\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M41.503 31.516 28.308 23.89M39.064 32.923l-10.757-6.217\"/\u003e\u003c/g\u003e\u003cpath d=\"m28.308 23.89-13.192 7.613\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m15.116 31.503.002 15.24M17.555 32.911l.002 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"M15.118 46.743 4.442 52.905M15.118 46.743l13.195 7.627\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.313 54.37 13.192-7.614M28.314 51.554l10.752-6.206\"/\u003e\u003c/g\u003e\u003cpath d=\"m41.503 31.516.002 15.24\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M83.022 26.344h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.018-.327-.023-.476q-.006-.262-.006-.483v-2.768h.577zM87.328 26.344h-.619v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M56.959 8.659q0 .757-.256 1.328-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.757-.887-.244-.571-.244-1.333 0-.751.244-1.31.251-.566.757-.881t1.273-.316q.733 0 1.233.316.5.309.756.875.256.565.256 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-.524-1.209-.524-.833 0-1.226.524t-.393 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#90e050\" stroke=\"none\" d=\"M1.173 56.807H.56v-4.9h2.732v.542H1.173v1.738h1.994v.542H1.173z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m77.928 25.716-5.021 2.901M81.083 20.044l.001-5.695\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m57.977 6.769 4.959-2.865M54.698 12.584l-.001 5.659\" class=\"hi\"/\u003e\u003cpath stroke=\"#90e050\" d=\"m4.442 52.905 5.338-3.081\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1R,2R)-4-Fluorophenmetrazine"},{"SMILES":"C[C@@H]1NCCO[C@@H]1C1=CC=C(F)C=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 87.888 57.367\"\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 0h88v58H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath stroke=\"none\" d=\"M68.236 31.518h-.7L65.788 46.75h4.2z\" class=\"bond\"/\u003e\u003cpath d=\"m67.886 31.518 10.042-5.802M81.083 20.044l.003-11.39M81.086 8.654 67.895 1.038M67.895 1.038l-9.918 5.731M54.698 12.584l-.003 11.318M67.886 31.518l-13.191-7.616\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"m54.87 24.206-.35-.607-15.266 6.618 2.249 1.299v2.597z\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M41.503 31.516 28.308 23.89M39.064 32.923l-10.757-6.217\"/\u003e\u003c/g\u003e\u003cpath d=\"m28.308 23.89-13.192 7.613\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m15.116 31.503.002 15.24M17.555 32.911l.002 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"M15.118 46.743 4.442 52.905M15.118 46.743l13.195 7.627\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.313 54.37 13.192-7.614M28.314 51.554l10.752-6.206\"/\u003e\u003c/g\u003e\u003cpath d=\"m41.503 31.516.002 15.24\" class=\"bond\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M83.022 26.344h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.018-.327-.023-.476q-.006-.262-.006-.483v-2.768h.577zM87.328 26.344h-.619v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M56.959 8.659q0 .757-.256 1.328-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.757-.887-.244-.571-.244-1.333 0-.751.244-1.31.251-.566.757-.881t1.273-.316q.733 0 1.233.316.5.309.756.875.256.565.256 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-.524-1.209-.524-.833 0-1.226.524t-.393 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#90e050\" stroke=\"none\" d=\"M1.173 56.807H.56v-4.9h2.732v.542H1.173v1.738h1.994v.542H1.173z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m77.928 25.716-5.021 2.901M81.083 20.044l.001-5.695\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m57.977 6.769 4.959-2.865M54.698 12.584l-.001 5.659\" class=\"hi\"/\u003e\u003cpath stroke=\"#90e050\" d=\"m4.442 52.905 5.338-3.081\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1S,2R)-4-Fluorophenmetrazine"},{"SMILES":"C[C@H]1NCCO[C@H]1C1=CC=C(F)C=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 87.888 57.367\"\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 0h88v58H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M68.236 31.518h-.7M68.528 34.057h-1.284M68.82 36.595l-1.867.001M69.112 39.134h-2.45M69.404 41.672l-3.034.001M69.696 44.211h-3.617M69.988 46.749l-4.2.001\"/\u003e\u003c/g\u003e\u003cpath d=\"m67.886 31.518 10.042-5.802M81.083 20.044l.003-11.39M81.086 8.654 67.895 1.038M67.895 1.038l-9.918 5.731M54.698 12.584l-.003 11.318M67.886 31.518l-13.191-7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m54.87 24.206-.35-.607M52.817 25.727l-.642-1.111M50.764 27.249l-.933-1.617M48.711 28.77l-1.225-2.122M46.658 30.292l-1.516-2.628M44.605 31.814l-1.808-3.133M42.552 33.335l-2.099-3.638\"/\u003e\u003c/g\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M41.503 31.516 28.308 23.89M39.064 32.923l-10.757-6.217\"/\u003e\u003c/g\u003e\u003cpath d=\"m28.308 23.89-13.192 7.613\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m15.116 31.503.002 15.24M17.555 32.911l.002 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"M15.118 46.743 4.442 52.905M15.118 46.743l13.195 7.627\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.313 54.37 13.192-7.614M28.314 51.554l10.752-6.206\"/\u003e\u003c/g\u003e\u003cpath d=\"m41.503 31.516.002 15.24\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M83.022 26.344h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.018-.327-.023-.476q-.006-.262-.006-.483v-2.768h.577zM87.328 26.344h-.619v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M56.959 8.659q0 .757-.256 1.328-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.757-.887-.244-.571-.244-1.333 0-.751.244-1.31.251-.566.757-.881t1.273-.316q.733 0 1.233.316.5.309.756.875.256.565.256 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-.524-1.209-.524-.833 0-1.226.524t-.393 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#90e050\" stroke=\"none\" d=\"M1.173 56.807H.56v-4.9h2.732v.542H1.173v1.738h1.994v.542H1.173z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m77.928 25.716-5.021 2.901M81.083 20.044l.001-5.695\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m57.977 6.769 4.959-2.865M54.698 12.584l-.001 5.659\" class=\"hi\"/\u003e\u003cpath stroke=\"#90e050\" d=\"m4.442 52.905 5.338-3.081\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1R,2S)-4-Fluorophenmetrazine"},{"SMILES":"C[C@@H]1NCCO[C@H]1C1=CC=C(F)C=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 87.888 57.367\"\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 0h88v58H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M68.236 31.518h-.7L65.788 46.75h4.2z\" class=\"bond\"/\u003e\u003cpath d=\"m67.886 31.518 10.042-5.802M81.083 20.044l.003-11.39M81.086 8.654 67.895 1.038M67.895 1.038l-9.918 5.731M54.698 12.584l-.003 11.318M67.886 31.518l-13.191-7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m54.87 24.206-.35-.607M52.817 25.727l-.642-1.111M50.764 27.249l-.933-1.617M48.711 28.77l-1.225-2.122M46.658 30.292l-1.516-2.628M44.605 31.814l-1.808-3.133M42.552 33.335l-2.099-3.638\"/\u003e\u003c/g\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M41.503 31.516 28.308 23.89M39.064 32.923l-10.757-6.217\"/\u003e\u003c/g\u003e\u003cpath d=\"m28.308 23.89-13.192 7.613\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m15.116 31.503.002 15.24M17.555 32.911l.002 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"M15.118 46.743 4.442 52.905M15.118 46.743l13.195 7.627\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.313 54.37 13.192-7.614M28.314 51.554l10.752-6.206\"/\u003e\u003c/g\u003e\u003cpath d=\"m41.503 31.516.002 15.24\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M83.022 26.344h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.018-.327-.023-.476q-.006-.262-.006-.483v-2.768h.577zM87.328 26.344h-.619v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M56.959 8.659q0 .757-.256 1.328-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.757-.887-.244-.571-.244-1.333 0-.751.244-1.31.251-.566.757-.881t1.273-.316q.733 0 1.233.316.5.309.756.875.256.565.256 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-.524-1.209-.524-.833 0-1.226.524t-.393 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#90e050\" stroke=\"none\" d=\"M1.173 56.807H.56v-4.9h2.732v.542H1.173v1.738h1.994v.542H1.173z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m77.928 25.716-5.021 2.901M81.083 20.044l.001-5.695\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m57.977 6.769 4.959-2.865M54.698 12.584l-.001 5.659\" class=\"hi\"/\u003e\u003cpath stroke=\"#90e050\" d=\"m4.442 52.905 5.338-3.081\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1S,2S)-4-Fluorophenmetrazine"}],"StereoisomerType":"diastereomer","Stereoisomers":["(1R,2R)-4-Fluorophenmetrazine","(1S,2R)-4-Fluorophenmetrazine","(1R,2S)-4-Fluorophenmetrazine","(1S,2S)-4-Fluorophenmetrazine"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 87.888 57.367\"\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 0h88v58H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m67.888 46.75-.002-15.232M67.886 31.518l-13.191-7.616M54.695 23.902l.003-11.318M57.977 6.769l9.918-5.731M67.895 1.038l13.191 7.616M81.086 8.654l-.003 11.39M67.886 31.518l10.042-5.802M54.695 23.902l-13.192 7.614\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M41.503 31.516 28.308 23.89M39.064 32.923l-10.757-6.217\"/\u003e\u003c/g\u003e\u003cpath d=\"m28.308 23.89-13.192 7.613\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m15.116 31.503.002 15.24M17.555 32.911l.002 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m15.118 46.743 13.195 7.627\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.313 54.37 13.192-7.614M28.314 51.554l10.752-6.206\"/\u003e\u003c/g\u003e\u003cpath d=\"m41.503 31.516.002 15.24M15.118 46.743 4.442 52.905\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M56.959 8.659q0 .757-.256 1.328-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.757-.887-.244-.571-.244-1.333 0-.751.244-1.31.251-.566.757-.881t1.273-.316q.733 0 1.233.316.5.309.756.875.256.565.256 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-.524-1.209-.524-.833 0-1.226.524t-.393 1.452\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M83.022 26.344h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.018-.327-.023-.476q-.006-.262-.006-.483v-2.768h.577zM87.328 26.344h-.619v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#90e050\" stroke=\"none\" d=\"M1.173 56.807H.56v-4.9h2.732v.542H1.173v1.738h1.994v.542H1.173z\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m54.698 12.584-.001 5.659M57.977 6.769l4.959-2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m81.083 20.044.001-5.695M77.928 25.716l-5.021 2.901\" class=\"hi\"/\u003e\u003cpath stroke=\"#90e050\" d=\"m4.442 52.905 5.338-3.081\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"4-Fluorophenmetrazine","UNII":"AEU8Y7H4Q6","XLogP":1.5}
