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氟矽唑

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氟矽唑
IUPAC名
1[Bis(4-fluorophenyl)(methyl)silyl]methyl1H-1,2,4-triazole
別名 DPX-H6573;
識別
CAS號 85509-19-9  checkY
PubChem 73675
ChemSpider 66326
SMILES
 
  • c2ncnn2C[Si](C)(c(cc1)ccc1F)c3ccc(F)cc3
InChI
 
  • 1/C16H15F2N3Si/c1-22(12-21-11-19-10-20-21,15-6-2-13(17)3-7-15)16-8-4-14(18)5-9-16/h2-11H,12H2,1H3
InChIKey FQKUGOMFVDPBIZ-UHFFFAOYAI
ChEBI 81922
性質
化學式 C16H15F2N3Si
莫耳質量 315.392 g/mol g·mol⁻¹
溶解性 41.9 mg/L (20°C)
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。

氟矽唑DPX-H6573)是一種由杜邦發明的有機矽殺真菌劑,用來控制各種水果和蔬菜農作物的真菌感染。[1][2][3]它對動物有中度毒性,大量攝入後可能會導致先天性障礙[4][5]

外部鏈接

[編輯]
  • 氟矽唑 in the Pesticide Properties DataBase (PPDB)

參考文獻

[編輯]
  1. ^ Moberg, W. K.; Basarab, G. S.; Cuomo, J.; Liang, P. H. Biologically Active Organosilicon Compounds. Synthesis and Chemistry of Agrochemicals. ACS Symposium Series 355. 1987: 288–301. ISBN 9780841214347. doi:10.1021/bk-1987-0355.ch026. 
  2. ^ Bostanian NJ, Larocque N, Chouinard G, Coderre D. Baseline toxicity of several pesticides to Hyaliodes vitripennis (Say) (Hemiptera: Miridae). Pest Management Science. November 2001, 57 (11): 1007–10. PMID 11721516. doi:10.1002/ps.374. 
  3. ^ Eckert MR, Rossall S, Selley A, Fitt BD. Effects of fungicides on in vitro spore germination and mycelial growth of the phytopathogens Leptosphaeria maculans and L. biglobosa (phoma stem canker of oilseed rape). Pest Management Science. April 2010, 66 (4): 396–405. PMID 20013877. doi:10.1002/ps.1890可免費查閱. 
  4. ^ Farag AT, Ibrahim HH. Developmental toxic effects of antifungal flusilazole administered by gavage to mice. Birth Defects Research Part B: Developmental and Reproductive Toxicology. February 2007, 80 (1): 12–7. PMID 17187383. doi:10.1002/bdrb.20098. 
  5. ^ Hermsen SA, van den Brandhof EJ, van der Ven LT, Piersma AH. Relative embryotoxicity of two classes of chemicals in a modified zebrafish embryotoxicity test and comparison with their in vivo potencies. Toxicology in Vitro. January 2011, 25 (3): 745–753. PMID 21238576. doi:10.1016/j.tiv.2011.01.005可免費查閱.