Oxycarboxin

Oxycarboxin
Names
	Preferred IUPAC name 6-Methyl-4,4-dioxo-N-phenyl-3,4-dihydro-2H-1,4λ6-oxathiine-5-carboxamide
	Other names Oxycarboxine; Dcmod; Oxicarboxin, Vitavax sulfone, Plantvax, Carbojet, 5,6-dihydro-2-methyl-1,4-oxathi-ine-3-carboxanilide-4,4-dioxide
Identifiers
CAS Number	5259-88-1;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:7858;
ChEMBL	ChEMBL1712057;
ChemSpider	20048;
ECHA InfoCard	100.023.697
KEGG	C10956;
PubChem CID	21330;
UNII	NPU5GBN17X;
CompTox Dashboard (EPA)	DTXSID8034792 ;
	InChI InChI=1S/C12H13NO4S/c1-9-11(18(15,16)8-7-17-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14) Key: AMEKQAFGQBKLKX-UHFFFAOYSA-N;
	SMILES CC1=C(S(=O)(=O)CCO1)/C(=N\c2ccccc2)/O;
Properties
Chemical formula	C12H13NO4S
Molar mass	267.30 g·mol−1
Melting point	120 °C (248 °F; 393 K)
Solubility in water	moderate
Solubility	acetone, DMF, ethanol, and methanol
Related compounds
Related compounds	, Triclopyr
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Oxycarboxin is an organic compound used as a fungicide.^[1]^[2] It is an anilide.^[3]

Uses[]

Oxycarboxin is used to control rust diseases (e.g. soybean rust).^[2]

Oxycarboxin has been commercially available since 1966.^[1]

Oxycarboxin is prepared from acetoacetanilide and 2-mercaptoethanol.^[1]

^ ^a ^b ^c Ackermann, Peter; Margot, Paul; Müller, Franz (2000). "Fungicides, Agricultural". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a12_085. ISBN 3527306730.
^ ^a ^b Shanmugasundaram, S.; Yeh, C.C.; Hartman, G.L.; Talekar, N.S. (1991). Vegetable Soybean Research Needs for Production and Quality Improvement (PDF). Taipei: Asian Vegetable Research and Development Center. pp. 86–87. ISBN 9789290580478. Retrieved 6 February 2016.
^ PubChem. "Oxycarboxin". PubChem. National Center for Biotechnology Information. Retrieved 2020-12-06.

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