25C-NBOMe

25C-NBOMe
法律規範狀態
法律規範	德：Anlage I; 英：Class A; 美：附表I; UN：Psychotropic Schedule I;
識別資訊
	IUPAC命名法 2-(4-Chloro-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl)methyl]ethan-1-amine; ;
CAS號	1227608-02-7
PubChem CID	46856354;
ChemSpider	24583389 ;
UNII	9FGW3C260N;
KEGG	C22720 ;
CompTox Dashboard（英語：CompTox Chemicals Dashboard） (EPA)	DTXSID10676790 ;
化學資訊
化學式	C18H22ClNO3
摩爾質量	335.83 g·mol−1
3D模型（JSmol（英語：JSmol））	交互式圖像;
	SMILES COc2ccccc2CNCCc(cc1OC)c(OC)cc1Cl;
	InChI InChI=1S/C18H22ClNO3/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 ; Key:FJFPOGCVVLUYAQ-UHFFFAOYSA-N ;

25C-NBOMe或稱為NBOMe-2C-C、2C-C-NBOMe、Cimbi-82是一種含氮有機氯化合物，分子式C
18H
22ClNO
3，是苯乙胺類化合物 2C-C（2,5-二甲氧基-4-氯苯乙胺）的25-NB類衍生物之一^[3]，能作為5-HT_2A受體的激動劑^[4]。

參考文獻

^ Substance Details 25C-NBOMe. [2024-01-23].
^ Anvisa. RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial [Collegiate Board Resolution No. 804 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control]. Diário Oficial da União. 2023-07-24 (2023-07-25) [2023-08-27]. （原始內容存檔於2023-08-27）（巴西葡萄牙語）.
^ Ettrup A, Hansen M, Santini MA, Paine J, Gillings N, Palner M, et al. Radiosynthesis and in vivo evaluation of a series of substituted 11C-phenethylamines as 5-HT (2A) agonist PET tracers. European Journal of Nuclear Medicine and Molecular Imaging. April 2011, 38 (4): 681–693. PMID 21174090. S2CID 12467684. doi:10.1007/s00259-010-1686-8.
^ Hansen M, Phonekeo K, Paine JS, Leth-Petersen S, Begtrup M, Bräuner-Osborne H, Kristensen JL. Synthesis and structure-activity relationships of N-benzyl phenethylamines as 5-HT2A/2C agonists. ACS Chemical Neuroscience. March 2014, 5 (3): 243–249. PMC 3963123 . PMID 24397362. doi:10.1021/cn400216u.