氯烯炔菊酯
外观
氯烯炔菊酯 | |
---|---|
识别 | |
CAS号 | 54407-47-5 |
SMILES |
|
性质 | |
化学式 | C16H20Cl2O2 |
摩尔质量 | 315.23 g·mol−1 |
外观 | 淡黄色油状液体[1] |
密度 | 1.192±0.06 g·cm−3[2] |
沸点 | 385.3±42.0 °C[2] |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
氯烯炔菊酯是一种有机化合物,化学式为C16H20Cl2O2。它是一种拟除虫菊酯杀虫剂,对蚊、蝇具有触杀活性。[1]它可由3-(2,2-二氯乙烯基)-2,2,-二甲基环丙酰氯(二氯菊酰氯)和4-甲基-4-庚烯-1-炔-3-醇在碳酸钾的存在下反应得到。[3][4]
参考文献
[编辑]- ^ 1.0 1.1 氯烯炔菊酯. ChemicalBook. [2020-07-01]. (原始内容存档于2020-07-03).
- ^ 2.0 2.1 Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (© 1994-2020 ACD/Labs). Retrieved from SciFinder. [2020-07-01]
- ^ Hidefumi Nakatsuji, Jun-ichi Morita, Tomonori Misaki, Yoo Tanabe. Water Solvent Method for Esterification and Amide Formation between Acid Chlorides and Alcohols Promoted by Combined Catalytic Amines: Synergy betweenN-Methylimidazole andN,N,N′,N′-Tetramethylethylenediamine (TMEDA). Advanced Synthesis & Catalysis. 2006-10, 348 (15): 2057–2062 [2020-07-01]. doi:10.1002/adsc.200600256 (英语).
- ^ Hidefumi Nakatsuji, Mami Morimoto, Tomonori Misaki, Yoo Tanabe. Mild, powerful, and robust methods for esterification, amide formation, and thioesterification between acid chlorides and alcohols, amines, thiols, respectively. Tetrahedron. 2007-11, 63 (48): 12071–12080 [2020-07-01]. doi:10.1016/j.tet.2007.08.117 (英语).