Davicil

Davicil
	Davicil skeletal structure
Names
	Preferred IUPAC name 2,3,5,6-Tetrachloro-4-(methanesulfonyl)pyridine
	Other names Tetrachloromethylsulfonylpyridine
Identifiers
CAS Number	13108-52-6 ;
3D model (JSmol)	Interactive image; Interactive image;
ChemSpider	55492 ;
ECHA InfoCard	100.032.744
PubChem CID	61579;
UNII	92AGR11YJB ;
CompTox Dashboard (EPA)	DTXSID4044795 ;
	InChI InChI=1S/C6H3Cl4NO2S/c1-14(12,13)4-2(7)5(9)11-6(10)3(4)8/h1H3 Key: NMCCNOZOBBWFMN-UHFFFAOYSA-N ; InChI=1/C6H3Cl4NO2S/c1-14(12,13)4-2(7)5(9)11-6(10)3(4)8/h1H3 Key: NMCCNOZOBBWFMN-UHFFFAOYAE;
	SMILES Clc1c(c(Cl)c(Cl)nc1Cl)S(=O)(=O)C; CS(=O)(=O)C1=C(C(=NC(=C1Cl)Cl)Cl)Cl;
Properties
Chemical formula	C6H3Cl4NO2S
Molar mass	294.970 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Davicil is a chlorinated pyridine derivative with antimicrobial properties, which is used as a fungicide. It can be allergenic in humans and produce contact dermatitis.^[1]^[2]

References

^ Oi M, Sumi K, Yokozeki H (January 2006). "Occupational allergy in office workers caused by the antifouling desk mat". Contact Dermatitis. 54 (1): 60–1. doi:10.1111/j.0105-1873.2006.0729c.x. PMID 16426296. S2CID 41411425.
^ Inoue T, Yagami A, Sano A, Nakagawa M, Abe M, Mori A, et al. (February 2008). "Contact dermatitis because of antimicrobial coating desk mat". Contact Dermatitis. 58 (2): 123–4. doi:10.1111/j.1600-0536.2007.01202.x. PMID 18186760. S2CID 5513569.

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