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 Y

3D model (JSmol)

* Interactive image
* Interactive image

ChemSpider |

* 55492 N

ECHA InfoCard | 100.032.744

PubChem CID

* 61579

UNII |

* 92AGR11YJB Y

CompTox Dashboard (EPA)

* DTXSID4044795

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

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).

N verify (what is YN ?)

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

[edit]

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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