{"Abbreviation":["3-MeO-PM"],"Aliases":["3-Meopm","PAL-823","Morpholine, 2-(3-methoxyphenyl)-3-methyl-","Unii-8vxk8lna5f","Schembl2599522","Dtxsid401343142"],"CAS":"1350768-49-8","ChemicalClasses":["2-phenylmorpholine"],"Chirality":"racemic","Erowid Experience Reports":[],"Esters":[],"Formating":[],"HeavyAtomCount":15,"IUPACName":"2-(3-methoxyphenyl)-3-methylmorpholine","InChI":"InChI=1S/C12H17NO2/c1-9-12(15-7-6-13-9)10-4-3-5-11(8-10)14-2/h3-5,8-9,12-13H,6-7H2,1-2H3","InChIKey":"QKAKYFBKVKSLLT-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e12\u003c/sub\u003eH\u003csub\u003e17\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"207.27 g/mol","Opticalactivity":"( + / - )","PubChemId":54673871,"Records":{"UNII":{"Impurities":[]}},"RefChem":"94654","RefCount":3,"RefCur":"","References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/54673871","Name":"3-Methoxyphenmetrazine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=1350768-49-8","Name":"3-Methoxyphenmetrazine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/8VXK8LNA5F","Name":"3-Methoxyphenmetrazine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID401343142","Name":"3-Methoxyphenmetrazine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 54673871, 3-methoxyphenmetrazine. Accessed May 12, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/54673871\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/54673871\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 3-Methoxyphenmetrazine. UNII: 8VXK8LNA5F. Global Substance Registration System. Accessed May 12, 2026. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/8VXK8LNA5F\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/8VXK8LNA5F\u003c/a\u003e"],"SMILES":"CC1C(OCCN1)C2=CC(=CC=C2)OC","SaltData":[],"Salts":[],"StereoisomerData":[{"SMILES":"COC1=CC=CC([C@H]2OCCN[C@@H]2C)=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 100.192 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=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h101v56H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m1.038 31.503 9.91-5.721M17.505 25.779l9.915 5.724\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.42 31.503.002 15.24M29.859 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