{"Abbreviation":["3-FPM","3F-Phenmetrazine"],"Aliases":["3-Fluorophenmetrazine","PAL-593","3-Fpm","Morpholine, 2-(3-fluorophenyl)-3-methyl-","Dtxsid201032414","Dtxcid101517419","2-(3-Fluorophenyl)-3-methyl-Morpholine","Unii-bev6rf569g","Schembl2599533","Schembl30457716","Chebi:191014","2-(3-luorophenyl)-3-methylmorpholine","NS00017993"],"CAS":"1350768-28-3","ChemicalClasses":["2-phenylmorpholine"],"Chirality":"racemic","DBI-IGS":["3-FPM","3-FPM"],"Dosing Info":[],"Erowid Experience Reports":[{"Author":"EthericBubble","Id":107056,"Title":"Rather Perfect"},{"Author":"Freddy","Id":105316,"Title":"Pleasant Mood Lifter"},{"Author":"Aldous","Id":107681,"Title":"Unsure What I Think"},{"Author":"bb","Id":111332,"Title":"FPM: Functional, Perfectly Manageable"},{"Author":"sunshine","Id":111419,"Title":"I Might as Well"},{"Author":"Mr._A","Id":108632,"Title":"The Buzz"},{"Author":"Magic_Raver","Id":104896,"Title":"Nice Energetic and Talkative Night"},{"Author":"Brad","Id":112907,"Title":"Pretty Fiendish and Habit Forming"},{"Author":"ThePoobaman","Id":113409,"Title":"Three Trials"},{"Author":"nervewing","Id":114265,"Title":"Awake and Awake"},{"Author":"RussianPsychonaut","Id":115071,"Title":"Three Days Awake"},{"Author":"Adude","Id":108583,"Title":"Moderate Binge"},{"Author":"uknaut93","Id":108344,"Title":"Clean and Clear Stimulant"},{"Author":"Bmorgs","Id":108162,"Title":"One Comfortable Stimulant"},{"Author":"Slappy_Bag","Id":105434,"Title":"In a Gaming Mood"},{"Author":"Jay_Dubwan","Id":105479,"Title":"Clean Long Lasting Stimulant"},{"Author":"Rocket","Id":107595,"Title":"SSRIs Take the Fun Out of It"},{"Author":"Anonymous","Id":113668,"Title":"A Worthwhile Aphrodisiac"},{"Author":"Lagrande","Id":113468,"Title":"High Working Libido"},{"Author":"SomeGuy","Id":106320,"Title":"A Worthy Adventure"},{"Author":"DIELATE","Id":106682,"Title":"The Coded Depths of Allylysergamide"},{"Author":"UndercoverPunk","Id":107673,"Title":"Increases Effects"},{"Author":"Toxicity_NA","Id":108056,"Title":"Must... Have... More..."},{"Author":"Ardougne","Id":115524,"Title":"Connecting With Gods and People's Energies"}],"Esters":[],"Formating":[],"HMDB ID":"HMDB0244559","HeavyAtomCount":14,"IUPACName":"2-(3-fluorophenyl)-3-methylmorpholine","InChI":"InChI=1S/C11H14FNO/c1-8-11(14-6-5-13-8)9-3-2-4-10(12)7-9/h2-4,7-8,11,13H,5-6H2,1H3","InChIKey":"VHYVKJAQSJCYCK-UHFFFAOYSA-N","MeSH Headers":[{"Id":"M000626901","Link":"https://id.nlm.nih.gov/mesh/M000626901.html","Name":"3-fluorophenmetrazine","Ref":14},{"Id":"DescTree","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":"MeSH Tree","Ref":16},{"Id":"PubMed from MeSH","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":null,"Ref":27}],"MolecularFormula":"C\u003csub\u003e11\u003c/sub\u003eH\u003csub\u003e14\u003c/sub\u003eFNO","MolecularWeight":"195.23 g/mol","Opticalactivity":"UNSPECIFIED","PD":"PD045019","PubChemId":54673723,"Record Description":["Wikipedia|List of designer drugs|Stimulants|Phenylmorpholines"],"Records":{"UNII":{"Impurities":[]}},"RefChem":"93965","RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/3-Fluorophenmetrazine","Name":"3-Fluorophenmetrazine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q20707008","Name":"3-Fluorophenmetrazine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/54673723","Name":"3-Fluorophenmetrazine","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD045019","Name":"3-Fluorophenmetrazine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=1350768-28-3","Name":"3-Fluorophenmetrazine","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0244559","Name":"3-Fluorophenmetrazine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/BEV6RF569G","Name":"3-Fluorophenmetrazine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID201032414","Name":"3-Fluorophenmetrazine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 54673723, 3-Fluorophenmetrazine. Accessed May 11, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/54673723\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/54673723\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 3-Fluorophenmetrazine. UNII: BEV6RF569G. Global Substance Registration System. Accessed May 11, 2026. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/BEV6RF569G\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/BEV6RF569G\u003c/a\u003e"],"SMILES":"CC1C(OCCN1)C2=CC(=CC=C2)F","SaltData":[],"Salts":[],"Scheduling":[{"gov":"Brazil","ref":[],"schedule":"F2 substance"},{"gov":"Canada","ref":[],"schedule":"Unscheduled substance"},{"act":"Neue-psychoaktive-Stoffe-Gesetz (NpSG)","gov":"Germany","ref":[],"schedule":"Neuer-Psychoaktiver-Stoff"},{"gov":"United Kingdom","ref":[],"schedule":"PSA substance"},{"gov":"United States","ref":[],"schedule":"Unscheduled; substance"}],"StereoisomerData":[{"SMILES":"C[C@H]1NCCO[C@@H]1C1=CC(F)=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 87.89 55.408\"\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 0h88v56H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M68.237 31.518h-.7M68.529 34.057h-1.283M68.821 36.595l-1.867.001M69.113 39.134h-2.45M69.405 41.672l-3.033.001M69.697 44.211H66.08M69.99 46.749l-4.201.001\"/\u003e\u003c/g\u003e\u003cpath d=\"m67.887 31.518 10.043-5.802M81.084 20.044l.004-11.39M81.088 8.654 67.897 1.038M67.897 1.038l-9.918 5.731M54.7 12.584l-.004 11.318M67.887 31.518l-13.191-7.616\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m54.871 24.206-.35-.607-15.266 6.618 2.249 1.299v2.597z\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M41.504 31.516 28.309 23.89M39.066 32.923l-10.758-6.217\"/\u003e\u003c/g\u003e\u003cpath d=\"m28.309 23.89-13.192 7.613M15.117 31.503l-10.95-6.322\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m15.117 31.503.003 15.24M17.556 32.911l.002 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m15.12 46.743 13.194 7.627\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.314 54.37 13.192-7.614M28.315 51.554l10.753-6.206\"/\u003e\u003c/g\u003e\u003cpath d=\"m41.504 31.516.002 15.24\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M83.023 26.344h-.72l-2.619-4.066h-.03l.03.595q.023.357.023.732v2.739h-.565v-4.9h.714l2.608 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM87.33 26.344h-.62v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.62z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M56.96 8.659q0 .757-.256 1.328-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.751.244-1.31.25-.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=\"#90e050\" stroke=\"none\" d=\"M1.173 26.337H.56v-4.899h2.732v.542H1.173v1.738h1.994v.542H1.173z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m77.93 25.716-5.021 2.901M81.084 20.044l.002-5.695\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m57.979 6.769 4.959-2.865M54.7 12.584l-.002 5.659\" class=\"hi\"/\u003e\u003cpath stroke=\"#90e050\" d=\"m4.167 25.181 5.475 3.161\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1R,2R)-3-Fluorophenmetrazine"},{"SMILES":"C[C@@H]1NCCO[C@@H]1C1=CC(F)=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 87.89 55.408\"\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 0h88v56H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath stroke=\"none\" d=\"M68.237 31.518h-.7L65.789 46.75h4.201z\" class=\"bond\"/\u003e\u003cpath d=\"m67.887 31.518 10.043-5.802M81.084 20.044l.004-11.39M81.088 8.654 67.897 1.038M67.897 1.038l-9.918 5.731M54.7 12.584l-.004 11.318M67.887 31.518l-13.191-7.616\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"m54.871 24.206-.35-.607-15.266 6.618 2.249 1.299v2.597z\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M41.504 31.516 28.309 23.89M39.066 32.923l-10.758-6.217\"/\u003e\u003c/g\u003e\u003cpath d=\"m28.309 23.89-13.192 7.613M15.117 31.503l-10.95-6.322\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m15.117 31.503.003 15.24M17.556 32.911l.002 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m15.12 46.743 13.194 7.627\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.314 54.37 13.192-7.614M28.315 51.554l10.753-6.206\"/\u003e\u003c/g\u003e\u003cpath d=\"m41.504 31.516.002 15.24\" class=\"bond\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M83.023 26.344h-.72l-2.619-4.066h-.03l.03.595q.023.357.023.732v2.739h-.565v-4.9h.714l2.608 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM87.33 26.344h-.62v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.62z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M56.96 8.659q0 .757-.256 1.328-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.751.244-1.31.25-.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=\"#90e050\" stroke=\"none\" d=\"M1.173 26.337H.56v-4.899h2.732v.542H1.173v1.738h1.994v.542H1.173z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m77.93 25.716-5.021 2.901M81.084 20.044l.002-5.695\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m57.979 6.769 4.959-2.865M54.7 12.584l-.002 5.659\" class=\"hi\"/\u003e\u003cpath stroke=\"#90e050\" d=\"m4.167 25.181 5.475 3.161\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1S,2R)-3-Fluorophenmetrazine"},{"SMILES":"C[C@H]1NCCO[C@H]1C1=CC(F)=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 87.89 55.408\"\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 0h88v56H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M68.237 31.518h-.7M68.529 34.057h-1.283M68.821 36.595l-1.867.001M69.113 39.134h-2.45M69.405 41.672l-3.033.001M69.697 44.211H66.08M69.99 46.749l-4.201.001\"/\u003e\u003c/g\u003e\u003cpath d=\"m67.887 31.518 10.043-5.802M81.084 20.044l.004-11.39M81.088 8.654 67.897 1.038M67.897 1.038l-9.918 5.731M54.7 12.584l-.004 11.318M67.887 31.518l-13.191-7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m54.871 24.206-.35-.607M52.818 25.727l-.642-1.111M50.765 27.249l-.933-1.617M48.712 28.77l-1.225-2.122M46.659 30.292l-1.516-2.628M44.607 31.814l-1.809-3.133M42.554 33.335l-2.1-3.638\"/\u003e\u003c/g\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M41.504 31.516 28.309 23.89M39.066 32.923l-10.758-6.217\"/\u003e\u003c/g\u003e\u003cpath d=\"m28.309 23.89-13.192 7.613M15.117 31.503l-10.95-6.322\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m15.117 31.503.003 15.24M17.556 32.911l.002 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m15.12 46.743 13.194 7.627\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.314 54.37 13.192-7.614M28.315 51.554l10.753-6.206\"/\u003e\u003c/g\u003e\u003cpath d=\"m41.504 31.516.002 15.24\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M83.023 26.344h-.72l-2.619-4.066h-.03l.03.595q.023.357.023.732v2.739h-.565v-4.9h.714l2.608 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM87.33 26.344h-.62v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.62z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M56.96 8.659q0 .757-.256 1.328-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.751.244-1.31.25-.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=\"#90e050\" stroke=\"none\" d=\"M1.173 26.337H.56v-4.899h2.732v.542H1.173v1.738h1.994v.542H1.173z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m77.93 25.716-5.021 2.901M81.084 20.044l.002-5.695\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m57.979 6.769 4.959-2.865M54.7 12.584l-.002 5.659\" class=\"hi\"/\u003e\u003cpath stroke=\"#90e050\" d=\"m4.167 25.181 5.475 3.161\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1R,2S)-3-Fluorophenmetrazine"},{"SMILES":"C[C@@H]1NCCO[C@H]1C1=CC(F)=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 87.89 55.408\"\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 0h88v56H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M68.237 31.518h-.7L65.789 46.75h4.201z\" class=\"bond\"/\u003e\u003cpath d=\"m67.887 31.518 10.043-5.802M81.084 20.044l.004-11.39M81.088 8.654 67.897 1.038M67.897 1.038l-9.918 5.731M54.7 12.584l-.004 11.318M67.887 31.518l-13.191-7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m54.871 24.206-.35-.607M52.818 25.727l-.642-1.111M50.765 27.249l-.933-1.617M48.712 28.77l-1.225-2.122M46.659 30.292l-1.516-2.628M44.607 31.814l-1.809-3.133M42.554 33.335l-2.1-3.638\"/\u003e\u003c/g\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M41.504 31.516 28.309 23.89M39.066 32.923l-10.758-6.217\"/\u003e\u003c/g\u003e\u003cpath d=\"m28.309 23.89-13.192 7.613M15.117 31.503l-10.95-6.322\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m15.117 31.503.003 15.24M17.556 32.911l.002 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m15.12 46.743 13.194 7.627\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.314 54.37 13.192-7.614M28.315 51.554l10.753-6.206\"/\u003e\u003c/g\u003e\u003cpath d=\"m41.504 31.516.002 15.24\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M83.023 26.344h-.72l-2.619-4.066h-.03l.03.595q.023.357.023.732v2.739h-.565v-4.9h.714l2.608 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM87.33 26.344h-.62v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.62z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M56.96 8.659q0 .757-.256 1.328-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.751.244-1.31.25-.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=\"#90e050\" stroke=\"none\" d=\"M1.173 26.337H.56v-4.899h2.732v.542H1.173v1.738h1.994v.542H1.173z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m77.93 25.716-5.021 2.901M81.084 20.044l.002-5.695\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m57.979 6.769 4.959-2.865M54.7 12.584l-.002 5.659\" class=\"hi\"/\u003e\u003cpath stroke=\"#90e050\" d=\"m4.167 25.181 5.475 3.161\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1S,2S)-3-Fluorophenmetrazine"}],"StereoisomerType":"diastereomer","Stereoisomers":["(1R,2R)-3-Fluorophenmetrazine","(1S,2R)-3-Fluorophenmetrazine","(1R,2S)-3-Fluorophenmetrazine","(1S,2S)-3-Fluorophenmetrazine"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 87.89 55.408\"\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 0h88v56H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m67.889 46.75-.002-15.232M67.887 31.518l-13.191-7.616M54.696 23.902l.004-11.318M57.979 6.769l9.918-5.731M67.897 1.038l13.191 7.616M81.088 8.654l-.004 11.39M67.887 31.518l10.043-5.802M54.696 23.902l-13.192 7.614\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M41.504 31.516 28.309 23.89M39.066 32.923l-10.758-6.217\"/\u003e\u003c/g\u003e\u003cpath d=\"m28.309 23.89-13.192 7.613\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m15.117 31.503.003 15.24M17.556 32.911l.002 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m15.12 46.743 13.194 7.627\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.314 54.37 13.192-7.614M28.315 51.554l10.753-6.206\"/\u003e\u003c/g\u003e\u003cpath d=\"m41.504 31.516.002 15.24M15.117 31.503l-10.95-6.322\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M56.96 8.659q0 .757-.256 1.328-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.751.244-1.31.25-.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=\"M83.023 26.344h-.72l-2.619-4.066h-.03l.03.595q.023.357.023.732v2.739h-.565v-4.9h.714l2.608 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.577zM87.33 26.344h-.62v-2.286h-2.512v2.286h-.613v-4.9h.613v2.072h2.512v-2.072h.62z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#90e050\" stroke=\"none\" d=\"M1.173 26.337H.56v-4.899h2.732v.542H1.173v1.738h1.994v.542H1.173z\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m54.7 12.584-.002 5.659M57.979 6.769l4.959-2.865\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m81.084 20.044.002-5.695M77.93 25.716l-5.021 2.901\" class=\"hi\"/\u003e\u003cpath stroke=\"#90e050\" d=\"m4.167 25.181 5.475 3.161\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"3-Fluorophenmetrazine","UNII":"BEV6RF569G","Wikidata":"Q20707008","Wikipedia":"3-Fluorophenmetrazine","XLogP":1.5}