{"Abbreviation":["25B-NBOMe"],"Aliases":["25B-NBOMe","Cimbi-36","RefChem:483953","2-(4-Bromo-2,5-dimethoxyphenyl)-N-(2-methoxybenzyl)ethanamine","4-bromo-2,5-dimethoxy-N-(2-methoxybenzyl)phenethylamine","2-(4-bromo-2,5-dimethoxyphenyl)-N-(2-methoxybenzyl)ethan-1-amine","4-bromo-2,5-dimethoxy-N-((2-methoxyphenyl)methyl)benzeneethanamine","4-Bromo-2,5-dimethoxy-N-[(2-methoxyphenyl)methyl]benzeneethanamine","New Nexus","2-(4-bromo-2,5-dimethoxyphenyl)-N-((2-methoxyphenyl)methyl)ethanamine","NBOMe-2C-B","BOM 2-CB","25-B-NBOMe","C22773","2,5-Dimethoxy-4-bromo-n-(2-methoxybenzyl)phenethylamine","2-(4-Bromo-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl)methyl]ethan-1-amine","Benzeneethanamine, 4-bromo-2,5-dimethoxy-n-((2-methoxyphenyl)methyl)-","Benzeneethanamine, 4-bromo-2,5-dimethoxy-N-[(2-methoxyphenyl)methyl]-; 4-Bromo-2,5-dimethoxy-N-[(2-methoxyphenyl)methyl]benzeneethanamine; 25B-NBOMe; 2C-B-NBOMe"],"CAS":"1026511-90-9","ChEMBL":"CHEMBL3590188","ChemicalClasses":["N-(2-methoxybenzyl)phenethylamine"],"Chirality":"achiral","Classes":["Psychedelic"],"DEA no":7536,"Esters":[],"European Community (EC) Number":"959-397-2","Formating":[],"HeavyAtomCount":23,"IUPACName":"2-(4-bromo-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl)methyl]ethanamine","InChI":"InChI=1S/C18H22BrNO3/c1-21-16-7-5-4-6-14(16)12-20-9-8-13-10-18(23-3)15(19)11-17(13)22-2/h4-7,10-11,20H,8-9,12H2,1-3H3","InChIKey":"SUXGNJVVBGJEFB-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e18\u003c/sub\u003eH\u003csub\u003e22\u003c/sub\u003eBrNO\u003csub\u003e3\u003c/sub\u003e","MolecularWeight":"380.3 g/mol","PD":"PD046561","PubChemId":9977044,"Record Description":["25B-NBOMe (NBOMe-2C-B, Cimbi-36, Nova, BOM 2-CB) is a derivative of the phenethylamine psychedelic 2C-B, discovered in 2004 by Ralf Heim at the Free University of Berlin. It acts as a potent partial agonist for the 5HT2A receptor. Anecdotal reports from users(citation needed) suggest 25B-NBOMe to be an active hallucinogen at a dose of as little as 250500 undefinedg,(citation needed) making it a similar potency to other phenethylamine derived hallucinogens such as bromo-dragonfly. Duration of effects lasts about 1216 hours.","Wikipedia|List of designer drugs|Psychedelics|NBxx"],"RefCount":4,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/25B-NBOMe","Name":"2,5-Dimethoxy-4-bromo-N-(2-methoxybenzyl)phenethylamine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q4632126","Name":"2,5-Dimethoxy-4-bromo-N-(2-methoxybenzyl)phenethylamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/9977044","Name":"2,5-Dimethoxy-4-bromo-N-(2-methoxybenzyl)phenethylamine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL3590188","Name":"2,5-Dimethoxy-4-bromo-N-(2-methoxybenzyl)phenethylamine","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD046561","Name":"2,5-Dimethoxy-4-bromo-N-(2-methoxybenzyl)phenethylamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=1026511-90-9","Name":"2,5-Dimethoxy-4-bromo-N-(2-methoxybenzyl)phenethylamine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C22773","Name":"2,5-Dimethoxy-4-bromo-N-(2-methoxybenzyl)phenethylamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/S6NAA81PHK","Name":"2,5-Dimethoxy-4-bromo-N-(2-methoxybenzyl)phenethylamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID50907974","Name":"2,5-Dimethoxy-4-bromo-N-(2-methoxybenzyl)phenethylamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 9977044, 2,5-Dimethoxy-4-bromo-N-(2-methoxybenzyl)phenethylamine. Accessed October 6, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/9977044\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/9977044\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-bromo-N-(2-methoxybenzyl)phenethylamine. UNII: S6NAA81PHK. Global Substance Registration System. Accessed October 6, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/S6NAA81PHK\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/S6NAA81PHK\u003c/a\u003e","Anvisa. RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial. Diário Oficial da União. July 24, 2023. Accessed October 6, 2025. \u003ca href=https://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-804-de-24-de-julho-de-2023-498447451\u003ehttps://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-804-de-24-de-julho-de-2023-498447451\u003c/a\u003e"],"SMILES":"COC1=CC=CC=C1CNCCC2=CC(=C(C=C2OC)Br)OC","SaltData":[],"Salts":[],"Scheduling":[{"gov":"Brazil","ref":["3"],"schedule":"F2 substance"},{"gov":"United Kingdom","ref":[],"schedule":"Class A substance"},{"act":"Controlled Substances Act (CSA)","gov":"United States","ref":[],"schedule":"Schedule I"},{"gov":"Germany","ref":[],"schedule":"Anlage I substance"},{"act":"Convention on Psychotropic Substances 1971","gov":"United Nations","ref":[],"schedule":"Schedule I drug"}],"StereoisomerData":[],"Stereoisomers":[],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 139.057 78.308\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the 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