{"Abbreviation":["25B-NBOH"],"Aliases":["2,5-Dimethoxy-4-bromo-N-(2-hydroxybenzyl)phenethylamine","2C-B-NBOH","NBOH-2C-B","25B-NBOH","2-((4-Bromo-2,5-dimethoxyphenethylamino)methyl)phenol","2-({[2-(4-bromo-2,5-dimethoxyphenyl)ethyl]amino}methyl)phenol","2-[[[2-(4-Bromo-2,5-dimethoxyphenyl)ethyl]amino]methyl]phenol","4-Bromo-2,5-dimethoxy-(n-(2-hydroxybenzyl))phenethylamine","Phenol, 2-[[[2-(4-bromo-2,5-dimethoxyphenyl)ethyl]amino]methyl]-","2-(((2-(4-Bromo-2,5-dimethoxyphenyl)ethyl)amino)methyl)phenol","Phenol, 2-(((2-(4-bromo-2,5-dimethoxyphenyl)ethyl)amino)methyl)-","RefChem:89918","2-(((4-bromo-2,5-dimethoxyphenethyl)amino)methyl)phenol"],"CAS":"1335331-46-8","ChemicalClasses":["N-(2-hydroxybenzyl)phenethylamine"],"Chirality":"achiral","Classes":["Psychedelic"],"Esters":[],"Formating":[],"HeavyAtomCount":22,"IUPACName":"2-[[2-(4-bromo-2,5-dimethoxyphenyl)ethylamino]methyl]phenol","InChI":"InChI=1S/C17H20BrNO3/c1-21-16-10-14(18)17(22-2)9-12(16)7-8-19-11-13-5-3-4-6-15(13)20/h3-6,9-10,19-20H,7-8,11H2,1-2H3","InChIKey":"RSUNJYKZRKIBNB-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e17\u003c/sub\u003eH\u003csub\u003e20\u003c/sub\u003eBrNO\u003csub\u003e3\u003c/sub\u003e","MolecularWeight":"366.2 g/mol","PD":"PD044688","PubChemId":125181394,"Record Description":["25B-NBOH (2C-B-NBOH, NBOH-2C-B) is a derivative of the phenethylamine derived hallucinogen 2C-B which has been sold as a designer drug. It acts as a potent serotonin receptor agonist with similar affinity to the better-known compound 25B-NBOMe at 5-HT2A and 5-HT2C receptors with pKis values of 8.3 and 9.4, respectively.","Wikipedia|List of designer drugs|Psychedelics|NBxx"],"RefCount":4,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/25B-NBOH","Name":"2,5-Dimethoxy-4-bromo-N-(2-hydroxybenzyl)phenethylamine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q20706992","Name":"2,5-Dimethoxy-4-bromo-N-(2-hydroxybenzyl)phenethylamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/125181394","Name":"2,5-Dimethoxy-4-bromo-N-(2-hydroxybenzyl)phenethylamine","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD044688","Name":"2,5-Dimethoxy-4-bromo-N-(2-hydroxybenzyl)phenethylamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=1335331-46-8","Name":"2,5-Dimethoxy-4-bromo-N-(2-hydroxybenzyl)phenethylamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/KHR1SJ9L0Y","Name":"2,5-Dimethoxy-4-bromo-N-(2-hydroxybenzyl)phenethylamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID401017175","Name":"2,5-Dimethoxy-4-bromo-N-(2-hydroxybenzyl)phenethylamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 125181394, 2,5-Dimethoxy-4-bromo-N-(2-hydroxybenzyl)phenethylamine. Accessed October 7, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/125181394\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/125181394\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-bromo-N-(2-hydroxybenzyl)phenethylamine. UNII: KHR1SJ9L0Y. Global Substance Registration System. Accessed October 7, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/KHR1SJ9L0Y\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/KHR1SJ9L0Y\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 7, 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(=C(C=C1CCNCC2=CC=CC=C2O)OC)Br","SaltData":[],"Salts":[],"Scheduling":[{"gov":"Brazil","ref":["3"],"schedule":"F2 substance"},{"act":"Neue-psychoaktive-Stoffe-Gesetz (NpSG)","gov":"Germany","ref":[],"schedule":"Neuer-Psychoaktiver-Stoff"},{"gov":"United Kingdom","ref":[],"schedule":"Class A substance"}],"StereoisomerData":[],"Stereoisomers":[],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 139.048 78.308\"\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\" 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