Chlortoluron

Chlortoluron
Names
	Preferred IUPAC name N'-(3-Chloro-4-methylphenyl)-N,N-dimethylurea
	Other names 3-(3-Chloro-4-methylphenyl)-1,1-dimethylurea
Identifiers
CAS Number	15545-48-9 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:81981 ;
ChemSpider	25472 ;
ECHA InfoCard	100.035.978
PubChem CID	27375;
UNII	SUW8L8G38A ;
CompTox Dashboard (EPA)	DTXSID8052853 ;
	InChI InChI=1S/C10H13ClN2O/c1-7-4-5-8(6-9(7)11)12-10(14)13(2)3/h4-6H,1-3H3,(H,12,14) Key: JXCGFZXSOMJFOA-UHFFFAOYSA-N ; InChI=1/C10H13ClN2O/c1-7-4-5-8(6-9(7)11)12-10(14)13(2)3/h4-6H,1-3H3,(H,12,14) Key: JXCGFZXSOMJFOA-UHFFFAOYAE;
	SMILES Clc1cc(NC(=O)N(C)C)ccc1C;
Properties
Chemical formula	C10H13ClN2O
Molar mass	212.67602
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

Chlortoluron is a phenylurea herbicide used to control broadleaf and annual grass weeds in cereal fields. [1][2]

Referenced

Lhomme, Ludovic; Brosillon, Stephan; Wolbert, Dominique; Dussaud, Joseph (2005). "Photocatalytic degradation of a phenylurea, chlortoluron, in water using an industrial titanium dioxide coated media". Applied Catalysis B: Environmental. 61 (3–4): 227–235. doi:10.1016/j.apcatb.2005.06.002.
Smith, A.E.; Briggs, G.G. (1978). "The fate of the herbicide chlortoluron and its possible degradation products in soils". Weed Research. 18 (1): 1–7. doi:10.1111/j.1365-3180.1978.tb01568.x.

gollark: It's great for bodging.

gollark: True, true.

gollark: That's... basically the main reason to use one.

gollark: They're useful for when you want to embed an interpreter in things.

gollark: It also probably wouldn't cause too many problems for them to actually include some (written in Lua) libraries with the standard distribution.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] Lhomme, Ludovic; Brosillon, Stephan; Wolbert, Dominique; Dussaud, Joseph (2005). "Photocatalytic degradation of a phenylurea, chlortoluron, in water using an industrial titanium dioxide coated media". Applied Catalysis B: Environmental. 61 (3–4): 227–235. doi:10.1016/j.apcatb.2005.06.002.

[2] Smith, A.E.; Briggs, G.G. (1978). "The fate of the herbicide chlortoluron and its possible degradation products in soils". Weed Research. 18 (1): 1–7. doi:10.1111/j.1365-3180.1978.tb01568.x.