Asulam - Misplaced Pages

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Asulam
Names

IUPAC name N-(4-Aminophenyl)sulfonylcarbamic acid methyl ester
Identifiers
CAS Number	3337-71-1
3D model (JSmol)	Interactive image
ChemSpider	17707
ECHA InfoCard	100.020.071
KEGG	C18350
PubChem CID	18752
CompTox Dashboard (EPA)	DTXSID8023890
InChI InChI=1S/C8H10N2O4S/c1-14-8(11)10-15(12,13)7-4-2-6(9)3-5-7/h2-5H,9H2,1H3,(H,10,11)Key: VGPYEHKOIGNJKV-UHFFFAOYSA-N InChI=1/C8H10N2O4S/c1-14-8(11)10-15(12,13)7-4-2-6(9)3-5-7/h2-5H,9H2,1H3,(H,10,11)Key: VGPYEHKOIGNJKV-UHFFFAOYAJ
SMILES O=S(=O)(c1ccc(N)cc1)NC(=O)OC
Properties
Chemical formula	C₈H₁₀N₂O₄S
Molar mass	230.241 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references

Chemical compound

Asulam is a herbicide invented by May & Baker Ltd, part of the Rhône-Poulenc Group, and internally called M&B9057 and used in horticulture and agriculture. It is used to kill bracken and docks also used as an antiviral agent. It is currently marketed, by United Phosphorus Ltd - UPL, as "Asulox" which contains 400 g/L of asulam sodium salt.

Asulam was declared not approved by the "Commission Implementing Regulation (EU) No 1045/2011 of 19 October 2011 concerning the non-approval of the active substance asulam, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Decision 2008/934/EC (http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2011:275:0023:0024:EN:PDF).

References

"ChemSpider". Retrieved 30 September 2011. {{cite web}}: Text "Asulam" ignored (help); Text "C8H10N2O4S" ignored (help)
R. J. Pakemana, M. G. Le Ducb and R. H. Marrs (1998). "An assessment of aerially applied asulam as a method of long-term bracken control". Journal of Environmental Management. 53 (3): 255–262. doi:10.1006/jema.1998.0207.
C. S. R. Snow and R. H. Marrs (1997). "Restoration of Calluna heathland on a bracken Pteridium-infested site in north west England". Biological Conservation. 81 (1–2): 35–42. doi:10.1016/S0006-3207(96)00147-4.
R. I. Speight and J. B. Whittaker (1987). "Interactions Between the Chrysomelid Beetle Gastrophysa viridula, the Weed Rumex obtusifolius and the Herbicide Asulam". The Journal of Applied Ecology. 24 (1). British Ecological Society: 119–129. doi:10.2307/2403791. JSTOR 2403791.

Pest control: herbicides

FOP herbicides	chlorazifop cyhalofop diclofop fenoxaprop fluazifop haloxyfop quizalofop
DIM herbicides	sethoxydim

Protox inhibitors

Nitrophenyl ethers	acifluorfen bifenox fluorodifen fomesafen lactofen nitrofen oxyfluorfen
Pyrimidinediones	butafenacil saflufenacil
Triazolinones	carfentrazone sulfentrazone

Pyridines

Quaternary

Photosystem I inhibitors	cyperquat diquat paraquat

Triazines

Photosystem II inhibitors	ametryn atrazine cyanazine hexazinone prometon prometryn propazine simazine simetryn terbuthylazine terbutryn metamitron

Ureas

Photosystem II inhibitors	chlortoluron DCMU difenoxuron isoproturon linuron monuron monolinuron tebuthiuron
ALS inhibitors	chlorsulfuron flazasulfuron metsulfuron-methyl sulfometuron methyl tribenuron

Others

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