Davicil
Davicil skeletal structure
Names
Preferred IUPAC name
2,3,5,6-Tetrachloro-4-(methanesulfonyl)pyridine
Other names
Tetrachloromethylsulfonylpyridine
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.032.744
UNII
  • 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
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).
☒N verify (what is checkY☒N ?)
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

  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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