ETHYL (2S)-(+)-2-[4-(6-CHLOROBENZOXAZOL-2-YLOXY)PHENOXY]PROP

ETHYL (2S)-(+)-2-[4-(6-CHLOROBENZOXAZOL-2-YLOXY)PHENOXY]PROPANOATE Basic information
Product Name:ETHYL (2S)-(+)-2-[4-(6-CHLOROBENZOXAZOL-2-YLOXY)PHENOXY]PROPANOATE
Synonyms:ETHYL (2S)-(+)-2-[4-(6-CHLOROBENZOXAZOL-2-YLOXY)PHENOXY]PROPANOATE;FENOXAPROP ETHYL
CAS:
MF:C18H16ClNO5
MW:361.78
EINECS:
Product Categories:
Mol File:Mol File
ETHYL (2S)-(+)-2-[4-(6-CHLOROBENZOXAZOL-2-YLOXY)PHENOXY]PROPANOATE Structure
ETHYL (2S)-(+)-2-[4-(6-CHLOROBENZOXAZOL-2-YLOXY)PHENOXY]PROPANOATE Chemical Properties
Safety Information
MSDS Information
ETHYL (2S)-(+)-2-[4-(6-CHLOROBENZOXAZOL-2-YLOXY)PHENOXY]PROPANOATE Usage And Synthesis
Metabolic pathwayA resistant biotype of Peldon A1 of Alopecurus myosuroides shows moderately enhanced metabolism of 14C-fenoxaprop ethyl. However, in the more resistant Lincs. E1, the metabolism rates of fenoxaprop ethyl are intermediate between Peldon A1 and the susceptible Rothamsted biotype. Fenoxaprop ethyl is hydrolyzed to the corresponding propionic acid which undergoes further degradation to give polar metabolites. The amounts of the metabolites depend on the metabolism activity of the individual biotypes. By wheat, barley, and crabgrass plants, fenoxaprop ethyl is de-esterified to fenoxaprop, resulting in a phytotoxic-free acid, 6-chloro-2,3-dihydrobenzoxazol-2-one, and 4-hydroxyphenoxypropionic acid.
ETHYL (2S)-(+)-2-[4-(6-CHLOROBENZOXAZOL-2-YLOXY)PHENOXY]PROPANOATE Preparation Products And Raw materials
Tag:ETHYL (2S)-(+)-2-[4-(6-CHLOROBENZOXAZOL-2-YLOXY)PHENOXY]PROPANOATE Related Product Information
FENOXAPROP-ETHYL FENOXAPROP