乙酰克里定
外觀
臨床資料 | |
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AHFS/Drugs.com | 國際藥品名稱 |
給藥途徑 | Topical (ophthalmic solution) |
ATC碼 | |
法律規範狀態 | |
法律規範 |
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藥物動力學數據 | |
藥物代謝 | deacetylation? |
識別資訊 | |
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CAS號 | 827-61-2 |
PubChem CID | |
ChemSpider | |
UNII | |
KEGG | |
ChEMBL | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.011.431 |
化學資訊 | |
化學式 | C9H15NO2 |
摩爾質量 | 169.22 g·mol−1 |
3D模型(JSmol) | |
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乙酰克里定或醋克利定是一種有機化合物,化學式為C9H15NO2。它可由3-喹核醇和乙酸酐反應製得。[1]它和3-溴溴苄反應,得到季銨鹽N-(3-溴苄基)乙酰克里定溴化物。[2]
參考文獻
[編輯]- ^ M. H. Shaw, V. W. Shurtleff, J. A. Terrett, J. D. Cuthbertson, D. W. C. MacMillan. Native functionality in triple catalytic cross-coupling: sp3 C-H bonds as latent nucleophiles. Science. 2016-06-10, 352 (6291): 1304–1308 [2021-08-15]. ISSN 0036-8075. PMC 5114852 . PMID 27127237. doi:10.1126/science.aaf6635 (英語).
- ^ Primozic, Ines; Bolant, Marijana; Ramic, Alma; Tomic, Srdanka. Preparation of novel meta and para substituted N-benzyl protected quinuclidine esters and their resolution with butyrylcholinesterase. International Electronic Conference on Synthetic Organic Chemistry, 15th, Nov. 1-30, 2011. ISBN 3-906980-25-1.