Dichlofluanid

Dichlofluanid
Names
	IUPAC name N-{[Dichloro(fluoro)methyl]sulfanyl}-N′,N′-dimethyl-N-phenylsulfuric diamide
Identifiers
CAS Number	1085-98-9 ;
3D model (JSmol)	Interactive image;
ChemSpider	13520;
ECHA InfoCard	100.012.835
PubChem CID	14145;
UNII	76A92XU36Y ;
CompTox Dashboard (EPA)	DTXSID5041851 ;
	InChI InChI=1S/C9H11Cl2FN2O2S2/c1-13(2)18(15,16)14(17-9(10,11)12)8-6-4-3-5-7-8/h3-7H,1-2H3 Key: WURGXGVFSMYFCG-UHFFFAOYSA-N; InChI=1/C9H11Cl2FN2O2S2/c1-13(2)18(15,16)14(17-9(10,11)12)8-6-4-3-5-7-8/h3-7H,1-2H3 Key: WURGXGVFSMYFCG-UHFFFAOYAE;
	SMILES CN(C)S(=O)(=O)N(C1=CC=CC=C1)SC(F)(Cl)Cl;
Properties
Chemical formula	C9H11Cl2FN2O2S2
Molar mass	333.22 g·mol−1
Density	1.55 g/cm3
Melting point	105–106 °C (221–223 °F; 378–379 K)
Hazards
	Lethal dose or concentration (LD, LC):
LD50 (median dose)	2500 mg/kg (rat)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Dichlofluanid (N-dichlorofluoromethylthio-N′, N′-dimethyl-N-phenylsulfamide) is a fungicide used to protect strawberries, grapes, berries, apples, pears and other fruit, vegetables and ornamental plants from diseases such as apple scab (Venturia inaequalis),^[2] black spot, leather rot, gray mold, downy mildew and others caused by the fungi Botrytis, Alternaria, Sclerotinia, and Monilinia. It is also used to protect against diseases of fruit during storage,^{[citation needed]} and as a wood preservative, often as part of a paint undercoat.^[3]

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Dichlofluanid was first marketed by Bayer Company in 1964, for use as a fungicide on plants.^[3] Its trade names include Euparen and Elvaron.^[1]

References