丙呋甲酮

丙呋甲酮
	IUPAC名; 1-[(2R)-2-(Prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]propan-1-one
识别
CAS号	4976-25-4
PubChem	78673
ChemSpider	71024
SMILES	O=C(C1=CC=C(O[C@@H](C(C)=C)C2)C2=C1)C;
InChI	1S/C13H14O2/c1-8(2)13-7-11-6-10(9(3)14)4-5-12(11)15-13/h4-6,13H,1,7H2,2-3H3/t13-/m1/s1;
InChIKey	UVYUUQGGBNKRFU-CYBMUJFWSA-N
性质
化学式	C13H14O2
摩尔质量	202.25 g·mol−1
	若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

丙呋甲酮（英語：Tremetone）是一种有机化合物，分子式C₁₃H₁₄O₂，存在于假藿香薊屬的物种（Ageratina altissima）中，有毒。^[1]^[2]^[3]^[4]

参考文献

^ Bonner, W. A. Ketones from "white snakeroot" Eupatorium urticaefolium. Tetrahedron. 1962, 18 (11): 1295–1309. doi:10.1016/0040-4020(62)80010-6.
^ Bowen, Douglas M.; Degraw, Joseph I.; Shah, Vinod R.; Bonner, William A. The Synthesis and Pharmacological Action of Tremetone. Journal of Medicinal Chemistry. 1963, 6 (3): 315–9. PMID 14185993. doi:10.1021/jm00339a023.
^ Bonner, W. A. The absolute configurations of tremetone and toxol. Tetrahedron. 1964, 20 (6): 1419–25. doi:10.1016/S0040-4020(01)99135-5.
^ Lee, Stephen T.; Davis, T. Zane; Gardner, Dale R.; Colegate, Steven M.; Cook, Daniel; Green, Benedict T.; Meyerholtz, Kimberly A.; Wilson, Christina R.; Stegelmeier, Bryan L.; Evans, Tim J. Tremetone and Structurally Related Compounds in White Snakeroot (Ageratina altissima): A Plant Associated with Trembles and Milk Sickness. Journal of Agricultural and Food Chemistry. 2010, 58 (15): 8560–5. PMID 20681643. doi:10.1021/jf1012456.

丙呋甲酮

IUPAC名 1-[(2R)-2-(Prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]propan-1-one
识别
CAS号	4976-25-4 ^Y
PubChem	78673
ChemSpider	71024
SMILES	O=C(C1=CC=C(O[C@@H](C(C)=C)C2)C2=C1)C
InChI	1S/C13H14O2/c1-8(2)13-7-11-6-10(9(3)14)4-5-12(11)15-13/h4-6,13H,1,7H2,2-3H3/t13-/m1/s1
InChIKey	UVYUUQGGBNKRFU-CYBMUJFWSA-N
性质
化学式	C₁₃H₁₄O₂
摩尔质量	202.25 g·mol⁻¹
若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。