2C-CN

2C-CN
臨床資料
其他名稱	25CN; 2,5-Dimethoxy-4-cyanophenethylamine; 4-Cyano-2,5-dimethoxyphenethylamine
識別資訊
	IUPAC命名法 4-(2-aminoethyl)-2,5-dimethoxybenzonitrile; ;
CAS號	88441-07-0
PubChem CID	57474247;
ChemSpider	28690053;
UNII	68O9X0114E;
CompTox Dashboard（英語：CompTox Chemicals Dashboard） (EPA)	DTXSID00726819 ;
化學資訊
化學式	C11H14N2O2
摩爾質量	206.25 g·mol−1
3D模型（JSmol（英語：JSmol））	交互式圖像;
	SMILES COC1=CC(=C(C=C1CCN)OC)C#N;
	InChI InChI=1S/C11H14N2O2/c1-14-10-6-9(7-13)11(15-2)5-8(10)3-4-12/h5-6H,3-4,12H2,1-2H3; Key:OGWCKYKYGQORLF-UHFFFAOYSA-N;

2C-CN，化學名：4-氰基-2,5-二甲氧基苯乙胺，（4-cyano-2,5-dimethoxyphenethylamine）是一種含氮有機化合物，化學式為C₁₁H₁₄N₂O₂，屬於2,5-二甲氧基苯乙胺衍生物（2C類化合物），最早在1984年的科學文獻中提出^[1]，亞歷山大·舒爾金在其書《PiHKAL》中也有描述^[2]。

參考文獻

^ Cheng AC, Castagnoli N. Synthesis and physicochemical and neurotoxicity studies of 1-(4-substituted-2,5-dihydroxyphenyl)-2-aminoethane analogues of 6-hydroxydopamine. Journal of Medicinal Chemistry. April 1984, 27 (4): 513–520. PMID 6423824. doi:10.1021/jm00370a014.
^ "The treatment of the 2C-B phthalimide described above, with cuprous cyanide rather than cuprous chloride, gave rise to the cyano analog which, on hydrolysis with hydrazine, yielded 2,5-dimethoxy-4-cyanophenethylamine (2C-CN). Hydrolysis of this with hot, strong base gave the corresponding acid, 2,5-dimethoxy-4-carboxyphenethylamine, 2C-COOH. No evaluation of either of these compounds has been made in the human animal, as far as I know."