氯烯炔菊酯
外觀
氯烯炔菊酯 | |
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識別 | |
CAS號 | 54407-47-5 |
SMILES |
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性質 | |
化學式 | C16H20Cl2O2 |
摩爾質量 | 315.23 g·mol−1 |
外觀 | 淡黃色油狀液體[1] |
密度 | 1.192±0.06 g·cm−3[2] |
沸點 | 385.3±42.0 °C[2] |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
氯烯炔菊酯是一種有機化合物,化學式為C16H20Cl2O2。它是一種擬除蟲菊酯殺蟲劑,對蚊、蠅具有觸殺活性。[1]它可由3-(2,2-二氯乙烯基)-2,2,-二甲基環丙醯氯(二氯菊醯氯)和4-甲基-4-庚烯-1-炔-3-醇在碳酸鉀的存在下反應得到。[3][4]
參考文獻
[編輯]- ^ 1.0 1.1 氯烯炔菊酯. ChemicalBook. [2020-07-01]. (原始內容存檔於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 (英語).
- ^ 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 (英語).