2-羟基苄胺

**2-HOBA**
识别信息
	IUPAC命名法 2-(aminomethyl)phenol; ;
CAS号	932-30-9
PubChem CID	70267;
ECHA InfoCard	100.012.045
化学信息
化学式	C7H9NO
摩尔质量	123.16 g·mol−1
3D模型（JSmol（英语：JSmol））	交互式图像;
	SMILES C1=CC=C(C(=C1)CN)O;
	InChI InChI=1S/C7H9NO/c8-5-6-3-1-2-4-7(6)9/h1-4,9H,5,8H2; Key:KPRZOPQOBJRYSW-UHFFFAOYSA-N;

2-羟基苄胺是一种有机化合物，化学式为C₇H₉NO。它可由碘化亚钐还原2-羟基苯甲腈制得。^[1]在碳酸钠存在下，它和氯乙酰氯反应，可以得到N-(2-羟基苄基)氯乙酰胺。^[2]它和二硫化碳在DMSO中反应，可以得到3,4-二氢-2H-1,3-苯并噁嗪-2-硫酮（）。^[3]

参考文献[编辑]

^ Gary A. Molander. John Wiley & Sons, Inc. , 编. Reductions with Samarium(II) Iodide. Hoboken, NJ, USA: John Wiley & Sons, Inc. 1994-10-27: 211–367 [2021-12-10]. ISBN 9780471264187. doi:10.1002/0471264180.or046.03. （原始内容存档于2022-02-27）（英语）.
^ Quinn P. Peterson, Danny C. Hsu, David R. Goode, Chris J. Novotny, Ryan K. Totten, Paul J. Hergenrother. Procaspase-3 Activation as an Anti-Cancer Strategy: Structure−Activity Relationship of Procaspase-Activating Compound 1 (PAC-1) and Its Cellular Co-Localization with Caspase-3. Journal of Medicinal Chemistry. 2009-09-24, 52 (18): 5721–5731 [2021-12-10]. ISSN 0022-2623. PMC 2749958 . PMID 19708658. doi:10.1021/jm900722z. （原始内容存档于2021-12-03）（英语）.
^ Chaochao Ding, Shaoli Wang, Yaoguang Sheng, Qian Dai, Yunjie Zhao, Guang Liang, Zengqiang Song. One-step construction of unsymmetrical thioureas and oxazolidinethiones from amines and carbon disulfide via a cascade reaction sequence. RSC Advances. 2019, 9 (46): 26768–26772 [2021-12-10]. ISSN 2046-2069. doi:10.1039/C9RA04540F （英语）.