1,4,5-萘三酚

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1,4,5-萘三酚
識別
CAS號 481-40-3  checkY
性質
化學式 C10H8O3
摩爾質量 176.17 g·mol−1
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。

1,4,5-萘三酚是一種有機化合物,化學式為C10H8O3。它可由5-羥基-1,4-萘醌連二亞硫酸鈉反應製得。[1]它可以被二(三氟乙酸)碘苯氧化為5-羥基-1,4-萘醌。[2]它和乙酸酐反應,可以得到1,4,5-萘三酚三乙酸酯。[3]

參考文獻[編輯]

  1. ^ Na Bao, Jinfeng Ou, Wei Shi, Na Li, Li Chen, Jianbo Sun. Highly Efficient Synthesis and Structure-Activity Relationships of a Small Library of Substituted 1,4-Naphthoquinones: Highly Efficient Synthesis and Structure-Activity Relationships of a Small Library of Substituted 1,4-Naphthoquinones. European Journal of Organic Chemistry. 2018-05-24, 2018 (19): 2254–2258 [2021-11-20]. doi:10.1002/ejoc.201800207 (英語). 
  2. ^ Robert M. Moriarty, Om Prakash. John Wiley & Sons, Inc. , 編. Oxidation of Phenolic Compounds with Organohypervalent Iodine Reagents. Hoboken, NJ, USA: John Wiley & Sons, Inc. 2001-05-18: 327–415 [2021-11-20]. ISBN 9780471264187. doi:10.1002/0471264180.or057.02. (原始內容存檔於2021-11-20) (英語). 
  3. ^ Mario C. Foti, Erin R. Johnson, Melinda R. Vinqvist, James S. Wright, L. Ross C. Barclay, K. U. Ingold. Naphthalene Diols: A New Class of Antioxidants Intramolecular Hydrogen Bonding in Catechols, Naphthalene Diols, and Their Aryloxyl Radicals. The Journal of Organic Chemistry. 2002-07-01, 67 (15): 5190–5196 [2021-11-20]. ISSN 0022-3263. doi:10.1021/jo020184v. (原始內容存檔於2021-11-20) (英語).