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 checkY
3D model (JSmol)
  • Interactive image
  • Interactive image
ChemSpider
  • 55492 ☒N
ECHA InfoCard 100.032.744 Edit this at Wikidata
PubChem CID
  • 61579
UNII
  • 92AGR11YJB checkY
CompTox Dashboard (EPA)
  • DTXSID4044795 Edit this at Wikidata
InChI
  • InChI=1S/C6H3Cl4NO2S/c1-14(12,13)4-2(7)5(9)11-6(10)3(4)8/h1H3 ☒N
    Key: NMCCNOZOBBWFMN-UHFFFAOYSA-N ☒N
  • InChI=1/C6H3Cl4NO2S/c1-14(12,13)4-2(7)5(9)11-6(10)3(4)8/h1H3
    Key: NMCCNOZOBBWFMN-UHFFFAOYAE
  • 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).
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Infobox references
Chemical compound

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

  1. ^ 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.
  2. ^ 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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