Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Chlordimeform

From Wikipedia, the free encyclopedia
Chlordimeform[1]
Names
IUPAC name
N-(4-chloro-2-methylphenyl)-N,N-dimethylmethanimidamide
Other names
Chlorphenamidine; Chlorfenamidine; Fundal; Galecron
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.025.637Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C10H13ClN2/c1-8-6-9(11)4-5-10(8)12-7-13(2)3/h4-7H,1-3H3 checkY
    Key: STUSTWKEFDQFFZ-UHFFFAOYSA-N checkY
  • InChI=1/C10H13ClN2/c1-8-6-9(11)4-5-10(8)12-7-13(2)3/h4-7H,1-3H3
    Key: STUSTWKEFDQFFZ-UHFFFAOYAO
  • Clc1cc(C)c(/N=C/N(C)C)cc1
Properties
C10H13ClN2
Molar mass196.68 g·mol−1
AppearanceWhite crystalline solid
Melting point32 °C (90 °F; 305 K) (225-227 °C, hydrochloride)
Boiling point163–165 °C
250 mg/L
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

Chlordimeform is anacaricide (pesticide) active mainly against motile forms ofmites andticks and against eggs and earlyinstars of someLepidoptera insects.[1] After theInternational Agency for Research on Cancer reported sufficient evidence that its major metabolite,4-chloro-o-toluidine, was acarcinogen, its use has ceased and its registration has been withdrawn in most countries.[1]

References

[edit]
  1. ^abcChlordimeform, International Program on Chemical Safety,World Health Organization
Carbamates
Inorganic compounds
Insect growth regulators
Neonicotinoids
Organochlorides
Organophosphorus
Pyrethroids
Diamides
Other chemicals
Metabolites
Biopesticides
Authority control databases: NationalEdit this at Wikidata


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=Chlordimeform&oldid=1292520544"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp