Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Tetradifon

From Wikipedia, the free encyclopedia
Tetradifon
Names
Preferred IUPAC name
1,2,4-Trichloro-5-(4-chlorobenzene-1-sulfonyl)benzene
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard100.003.759Edit this at Wikidata
EC Number
  • 204-134-2
KEGG
UNII
  • InChI=1S/C12H6Cl4O2S/c13-7-1-3-8(4-2-7)19(17,18)12-6-10(15)9(14)5-11(12)16/h1-6H ☒N
    Key: MLGCXEBRWGEOQX-UHFFFAOYSA-N ☒N
  • InChI=1/C12H6Cl4O2S/c13-7-1-3-8(4-2-7)19(17,18)12-6-10(15)9(14)5-11(12)16/h1-6H
    Key: MLGCXEBRWGEOQX-UHFFFAOYAO
  • C1=CC(=CC=C1S(=O)(=O)C2=CC(=C(C=C2Cl)Cl)Cl)Cl
Properties
C12H6Cl4O2S
Molar mass356.04 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Tetradifon is amiticide.[1] It acts by inhibitingmitochondrialATP synthase and is inIRAC group 12C.

References

[edit]
  1. ^Lippold, P. C (1966). "Comparison of Tetradifon Emulsifiable Concentrate and Wettable Powder Formulations Against the Two-Spotted Spider Mite".Journal of Economic Entomology.59 (2):303–306.doi:10.1093/jee/59.2.303.

External links

[edit]
  • Tetradifon in the Pesticide Properties DataBase (PPDB)
Carbamates
Inorganic compounds
Insect growth regulators
Neonicotinoids
Organochlorides
Organophosphorus
Pyrethroids
Diamides
Other chemicals
Metabolites
Biopesticides


Stub icon

This article about anorganic halide is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Tetradifon&oldid=1263267960"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp