Alloxydim

Chemical compound From Wikipedia, the free encyclopedia

Alloxydim is a chemical compound. Its formula is C17H25NO5. A member of the cyclohexanedione herbicide class, alloxydim is a post-emergence herbicide.[2] The sodium salt is a hygroscopic, water-soluble colorless solid.[3]

Quick facts Names, Identifiers ...
Alloxydim
Skeletal formula of alloxydim
Skeletal formula of alloxydim
Names
Preferred IUPAC name
Methyl 2-hydroxy-6,6-dimethyl-4-oxo-3-[(E)-N-prop-2-enoxy-C-propylcarbonimidoyl]cyclohex-2-ene-1-carboxylate
Other names
  • Carbodimedon
  • Zizalon
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.054.284 Edit this at Wikidata
EC Number
  • 259-732-6
UNII
  • InChI=1S/C17H25NO5/c1-6-8-11(18-23-9-7-2)13-12(19)10-17(3,4)14(15(13)20)16(21)22-5/h7,14,19H,2,6,8-10H2,1,3-5H3/b18-11+
    Key: ORFLOUYIJLPLPL-WOJGMQOQSA-N
  • CCC/C(=N\OCC=C)/C1=C(C(C(CC1=O)(C)C)C(=O)OC)O
Properties
C17H25NO5
Molar mass 323.389 g·mol−1
Hazards
Lethal dose or concentration (LD, LC):
  • 2260 mg/kg (rat, oral)[1]
  • >4300 mg/m3/4H (rat, inhalation)[1]
  • >5 g/kg (rat, skin)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Close

Alloxydim's HRAC classification is Group A (Australia and global), or Group 1 (numeric). Group A herbicides inhibit acetyl CoA carboxylase, (ACCase).[4]

Synthesis

Alloxydim may be produced by a multi-step reaction from mesityl oxide with dimethyl malonate, butyryl chloride, and o-ethylhydroxylamine.[5]

Uses

Alloxydim is a grass herbicide that acts by inhibiting acetyl-CoA carboxylase.[2] It was developed by Nippon Soda in 1976[6][7] and used from 1978 to 1992 in Germany.[8]

See also

References

Related Articles

Wikiwand AI