氟硅唑

氟硅唑
	IUPAC名; 1[Bis(4-fluorophenyl)(methyl)silyl]methyl1H-1,2,4-triazole
别名	DPX-H6573;
识别
CAS号	85509-19-9
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
性质
化学式	C16H15F2N3Si
摩尔质量	315.392 g/mol g·mol⁻¹
溶解性（水）	41.9 mg/L (20°C)
	若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

氟硅唑（DPX-H6573）是一种由杜邦发明的有机硅杀真菌剂，用来控制各种水果和蔬菜农作物的真菌感染。^[1]^[2]^[3]它对动物有中度毒性，大量摄入后可能会导致先天性障碍。^[4]^[5]

外部链接

^ 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.
^ 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.
^ 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 .
^ 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.
^ 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 .

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