4-苄基哌啶

4-苄基哌啶
法律规范状态
法律规范	德：The NpSG do not apply to this substance, because it is not a 2-Phenylethylamine derivative; 英：PSA;
识别信息
	IUPAC命名法 4-(phenylmethyl)piperidine; ;
CAS号	31252-42-3
PubChem CID	31738;
ChemSpider	29432 ;
UNII	JDF1T4667S;
ChEMBL	ChEMBL144129 ;
CompTox Dashboard（英语：CompTox Chemicals Dashboard） (EPA)	DTXSID3067603 ;
ECHA InfoCard	100.045.926
化学信息
化学式	C12H17N
摩尔质量	175.28 g·mol−1
3D模型（JSmol（英语：JSmol））	交互式图像;
	SMILES C1CNCCC1CC2=CC=CC=C2;
	InChI InChI=1S/C12H17N/c1-2-4-11(5-3-1)10-12-6-8-13-9-7-12/h1-5,12-13H,6-10H2 ; Key:ABGXADJDTPFFSZ-UHFFFAOYSA-N ;

4-苄基哌啶（化学式：C₁₂H₁₇N）是一种单胺释放剂，释放多巴胺的选择性是血清素的20到48倍。它可由哌啶和苯甲醛反应，再经催化氢化得到。^[1]它和三氟乙酸酐在二氯甲烷中反应，可以得到N-三氟甲酰基-4-苄基哌啶。^[2]

参考文献

^ Zeng Hong, Xin Ge, Shaodong Zhou. Underlying Mechanisms of Reductive Amination on Pd-Catalysts: The Unique Role of Hydroxyl Group in Generating Sterically Hindered Amine. International Journal of Molecular Sciences. 2022-07-10, 23 (14): 7621 [2023-03-07]. ISSN 1422-0067. doi:10.3390/ijms23147621. （原始内容存档于2022-10-01）（英语）.
^ Karine Alarcon, Adeline Martz, Laetitia Mony, Jacques Neyton, Pierre Paoletti, Maurice Goeldner, Bernard Foucaud. Reactive derivatives for affinity labeling in the ifenprodil site of NMDA receptors. Bioorganic & Medicinal Chemistry Letters. 2008-05, 18 (9): 2765–2770 [2023-03-07]. doi:10.1016/j.bmcl.2008.04.019. （原始内容存档于2022-08-02）（英语）.