{"Abbreviation":["DMCPA"],"Aliases":["DMCPA","2-(2,5-Dimethoxy-4-methylphenyl)cyclopropanamine","2-(2,5-dimethoxy-4-methylphenyl)cyclopropan-1-amine","Dmcpa, (1S,2R)-","49F6CJ4MFY","2,5-Dimethoxy-4-methylphenylcyclopropylamine, (1S,2R)-","Cyclopropanamine, 2-(2,5-dimethoxy-4-methylphenyl)-, (1S-trans)-","69980-36-5"],"CAS":"714903-64-7","ChemicalClasses":["phenylcyclopropylamine"],"Chirality":"achiral","Classes":["Psychedelic"],"DurationOfAction":"","EliminationHalfLife":"","Esters":[],"Formating":[],"HeavyAtomCount":15,"IUPACName":"trans-(1S,2R)-2-(2,5-dimethoxy-4-methylphenyl)cyclopropan-1-amine","InChI":"InChI=1S/C12H17NO2/c1-7-4-12(15-3)9(6-11(7)14-2)8-5-10(8)13/h4,6,8,10H,5,13H2,1-3H3/t8-,10+/m1/s1","InChIKey":"HYVPPECPQRBJEQ-SCZZXKLOSA-N","MolecularFormula":"C\u003csub\u003e12\u003c/sub\u003eH\u003csub\u003e17\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"207.27 g/mol","Opticalactivity":"( + / - )","PubChemId":92950747,"Record Description":["Wikipedia|PiHKAL|Phenethylamines"],"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/2,5-Dimethoxy-4-methylphenylcyclopropylamine","Name":"2,5-Dimethoxy-4-methylphenylcyclopropylamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/92950747","Name":"2,5-Dimethoxy-4-methylphenylcyclopropylamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=714903-64-7","Name":"2,5-Dimethoxy-4-methylphenylcyclopropylamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/U2YC8RFK7B","Name":"2,5-Dimethoxy-4-methylphenylcyclopropylamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 92950747, 2,5-Dimethoxy-4-methylphenylcyclopropylamine. Accessed October 9, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/92950747\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/92950747\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-methylphenylcyclopropylamine. UNII: U2YC8RFK7B. Global Substance Registration System. Accessed October 9, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/U2YC8RFK7B\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/U2YC8RFK7B\u003c/a\u003e"],"SMILES":"CC1=CC(=C(C=C1OC)[C@H]2C[C@@H]2N)OC","SaltData":[{"AcidCount":1,"Amine":"2,5-Dimethoxy-4-methylphenylcyclopropylamine","AmineCount":1,"Formula":"Cl","Name":"hydrochloride","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 127.69 60.881\"\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 0h128v61H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m14.241 44.725 13.199-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 37.105 13.203 7.628M29.877 35.697l10.766 6.221\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.643 44.733 13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.841 37.113-.005-15.248M51.402 35.706l-.004-12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 21.865-13.203-7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.633 14.236-13.198 7.62M40.632 17.052l-10.759 6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 37.105-.005-15.249M27.435 21.856l-9.924-5.727M10.955 16.133l-9.917 5.728\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m67.209 14.548-.35-.606-15.271 6.624 2.248 1.299v2.597z\" class=\"bond\"/\u003e\u003cpath d=\"m67.034 14.245 7.622-13.207M74.656 1.038l7.618 13.209M67.034 14.245l15.24.002M82.274 14.247l10.043 5.803M53.841 37.113l9.915 5.723M67.041 48.653l.002 11.318\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M16.494 14.236q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881t1.274-.316q.732 0 1.232.316.5.31.756.875.256.566.256 1.328m-3.863 0q0 .922.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M97.411 24.321h-.721l-2.619-4.066h-.03l.03.596q.024.357.024.732v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.327-.024-.477q-.006-.262-.006-.482v-2.768h.578zM101.717 24.321h-.619v-2.286h-2.512v2.286h-.614v-4.899h.614v2.072h2.512v-2.072h.619zM104.222 25.811h-1.943v-.3l.771-.779q.222-.221.372-.393.153-.175.232-.339.078-.168.078-.364 0-.243-.146-.368-.143-.129-.372-.129-.214 0-.378.075-.161.075-.329.207l-.193-.243q.172-.146.393-.246.225-.1.507-.1.411 0 .65.207t.24.575q0 .229-.097.432-.092.2-.264.397-.168.196-.393.418l-.614.603v.018h1.486z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M69.3 44.728q0 .756-.256 1.328-.256.565-.757.881-.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 1.232.316.501.309.757.875.256.565.256 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-.928-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.452\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m17.511 16.129 4.962 2.863M10.955 16.133l-4.958 2.864\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m92.317 20.05-5.021-2.902\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m63.756 42.836-4.957-2.862M67.041 48.653l.001 5.659\" class=\"hi\"/\u003e\u003c/g\u003e\u003cg class=\"mol\"\u003e\u003cg fill=\"#1ff01f\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M124.373 28.589q-.785 0-1.238.53-.452.524-.452 1.447 0 .911.416 1.446.423.53 1.268.53.322 0 .608-.053.291-.06.565-.143v.535q-.274.102-.565.149-.292.054-.697.054-.744 0-1.25-.31-.5-.309-.75-.875-.25-.571-.25-1.339 0-.744.268-1.31.274-.565.803-.881.53-.321 1.28-.321.78 0 1.352.285l-.244.524q-.227-.101-.506-.184-.274-.084-.608-.084m2.757 4.423h-.601v-5.214h.601zM121.466 33.012h-.619v-2.286h-2.512v2.286h-.613v-4.899h.613v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"2,5-Dimethoxy-4-methylphenylcyclopropylamine hydrochloride","UNII":"V9TT57FWR4"}],"Salts":["hydrochloride"],"Scheduling":[],"StereoisomerData":[],"Stereoisomers":[],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 104.782 60.881\"\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 0h105v61H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m14.241 44.725 13.199-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.44 37.105 13.203 7.628M29.877 35.697l10.766 6.221\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.643 44.733 13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.841 37.113-.005-15.248M51.402 35.706l-.004-12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.836 21.865-13.203-7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.633 14.236-13.198 7.62M40.632 17.052l-10.759 6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.44 37.105-.005-15.249M27.435 21.856l-9.924-5.727M10.955 16.133l-9.917 5.728\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m67.209 14.548-.35-.606-15.271 6.624 2.248 1.299v2.597z\" class=\"bond\"/\u003e\u003cpath d=\"m67.034 14.245 7.622-13.207M74.656 1.038l7.618 13.209M67.034 14.245l15.24.002M82.274 14.247l10.043 5.803M53.841 37.113l9.915 5.723M67.041 48.653l.002 11.318\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M16.494 14.236q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.244-.571-.244-1.333 0-.75.244-1.31.25-.566.756-.881t1.274-.316q.732 0 1.232.316.5.31.756.875.256.566.256 1.328m-3.863 0q0 .922.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M97.411 24.321h-.721l-2.619-4.066h-.03l.03.596q.024.357.024.732v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.327-.024-.477q-.006-.262-.006-.482v-2.768h.578zM101.717 24.321h-.619v-2.286h-2.512v2.286h-.614v-4.899h.614v2.072h2.512v-2.072h.619zM104.222 25.811h-1.943v-.3l.771-.779q.222-.221.372-.393.153-.175.232-.339.078-.168.078-.364 0-.243-.146-.368-.143-.129-.372-.129-.214 0-.378.075-.161.075-.329.207l-.193-.243q.172-.146.393-.246.225-.1.507-.1.411 0 .65.207t.24.575q0 .229-.097.432-.092.2-.264.397-.168.196-.393.418l-.614.603v.018h1.486z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M69.3 44.728q0 .756-.256 1.328-.256.565-.757.881-.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 1.232.316.501.309.757.875.256.565.256 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-.928-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.452\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m17.511 16.129 4.962 2.863M10.955 16.133l-4.958 2.864\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m92.317 20.05-5.021-2.902\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m63.756 42.836-4.957-2.862M67.041 48.653l.001 5.659\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Subjective Effects":null,"Title":"2,5-Dimethoxy-4-methylphenylcyclopropylamine","UNII":"U2YC8RFK7B","Wikipedia":"2,5-Dimethoxy-4-methylphenylcyclopropylamine","XLogP":1.5}