| Identification | Back Directory | [Name]
cycloxydim | [CAS]
99434-58-9 | [Synonyms]
(±)-2-(1-(ethoxyimino)butyl)-3-hydroxy-5-thian-3-ylcyclohex-2-enone
2-(1-ethoxyaminobutylidene)-5-(3-tetrahydrothiopyranyl)-cyclohexane-1,3-dione
1,3-Cyclohexanedione, 2-[1-(ethoxyamino)butylidene]-5-(tetrahydro-2H-thiopyran-3-yl)-
(±)-2-(1-(ethoxyimino)butyl)-3-hydroxy-5-(tetrahydro-2H-thiopyran-3-yl)-2-cyclohexene-1-one | [Molecular Formula]
C17H27NO3S | [MOL File]
99434-58-9.mol | [Molecular Weight]
325.47 |
| Hazard Information | Back Directory | [Chemical Properties]
Appearance is yellow solid. Soluble in various organic solvents and insoluble in water. | [Uses]
Cycloxydim is used for the control of annual and perennial grass weeds such as cotton, rape, soybean, potato and vegetable and other broad-leaved crops such as wild oats, ryegrass and ryegrass. | [Definition]
ChEBI: Cycloxydim is a beta-diketone that is cyclohexa-1,3-dione which is substituted at position 2 by an N-ethoxybutanimidoyl group and at position 5 by a tetrahydro-2H-thiopyran-3-yl group. A systemic herbicide effective against grasses, it is used in the cultivation of a variety of crops, including oil seed rape and potatoes. It has a role as an EC 6.4.1.2 (acetyl-CoA carboxylase) inhibitor, a herbicide, an agrochemical and a fatty acid synthesis inhibitor. It is an organosulfur heterocyclic compound, an oxime O-ether, a beta-diketone and an enol. | [Preparation]
Cycloxydim was prepared by reacting butyryl chloride reacts with 5-(thian-3-yl)-cyclohexan-1,3-dione and ethoxyamine hydrochloride in ethanol. |
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