Fludioxonil

Fludioxonil
Names
	IUPAC name 4-(2,2-Difluoro-1,3-benzodioxol-4-yl)-1H-pyrrole-3-carbonitrile
Identifiers
CAS Number	131341-86-1 ;
3D model (JSmol)	Interactive image;
ChemSpider	77916;
ECHA InfoCard	100.125.684
PubChem CID	86398;
UNII	ENS9J0YM16 ;
CompTox Dashboard (EPA)	DTXSID2032398 ;
	InChI InChI=1S/C12H6F2N2O2/c13-12(14)17-10-3-1-2-8(11(10)18-12)9-6-16-5-7(9)4-15/h1-3,5-6,16H Key: MUJOIMFVNIBMKC-UHFFFAOYSA-N; InChI=1/C12H6F2N2O2/c13-12(14)17-10-3-1-2-8(11(10)18-12)9-6-16-5-7(9)4-15/h1-3,5-6,16H Key: MUJOIMFVNIBMKC-UHFFFAOYAI;
	SMILES c1cc(c2c(c1)OC(O2)(F)F)c3c[nH]cc3C#N;
Properties
Chemical formula	C12H6F2N2O2
Molar mass	248.189 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Fludioxonil is a non-systemic fungicide, introduced in 1993 by Ciba-Geigy (now Syngenta). It is used for the treatment of crops (particularly cereals, fruits and vegetables, and ornamental plants; often in combination with another fungicide such as cyprodinil). Brand names include seed treatments: Celest, Agri Star Fludioxonil 41 ST, Dyna-shield Fludioxonil, Maxim 4 FS, and Spirato 480 FS, as well as foliar applications: Switch (fludioxonil + cyprodinil) [1]. Fludioxonil is used against Fusarium, Rhizoctonia, Alternaria and Botrytis cinerea.

It is toxic to fish and other aquatic organisms.[2]

Its mode of action is to inhibit transport-associated phosphorylation of glucose, which reduces mycelial growth rate.[3]

References

https://ipcm.wisc.edu/download/pubsPM/Whats_on_your_seed_web.pdf
Paranjape, Kalyani, Vasant Gowariker, V. N. Krishnamurthy, and Sugha Gowariker. The Pesticide Encyclopedia. CABI, 2014.
http://sitem.herts.ac.uk/aeru/ppdb/en/Reports/330.htm

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[1] ttps://ipcm.wisc.edu/download/pubsPM/Whats_on_your_seed_web.pdf

[2] Paranjape, Kalyani, Vasant Gowariker, V. N. Krishnamurthy, and Sugha Gowariker. The Pesticide Encyclopedia. CABI, 2014.

[3] ttp://sitem.herts.ac.uk/aeru/ppdb/en/Reports/330.htm