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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide
ChemicalBook CAS DataBase List Haloxyfop-P
95977-29-0

Haloxyfop-P synthesis

2synthesis methods
Haloxyfop-P tends to be used and produced as the methyl variant. The commercial production of haloxyfop-P-methyl involves a multi-step synthetic process designed to yield the biologically active R-enantiomer with high optical purity. It begins with the preparation of a substituted hydroquinone, which undergoes etherification with a chiral alkylating agent, typically (R)-2-bromopropionic acid methyl ester, to introduce the stereocentre. This intermediate is then reacted with a halogenated pyridine derivative, such as 3-chloro-2-bromo-5-trifluoromethylpyridine, under controlled conditions to form the key pyridyloxy linkage. The resulting compound is purified and esterified to produce haloxyfop-P-methyl.
2,3-Dichloro-5-(trifluoromethyl)pyridine

69045-84-7
414 suppliers
$10.00/5g

94050-90-5 Synthesis
(R)-(+)-2-(4-Hydroxyphenoxy)propionic acid

94050-90-5
344 suppliers
$6.00/10g

Haloxyfop-P

95977-29-0
63 suppliers
$36.70/25mg

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Haloxyfop-phenol Metabolite

69045-89-2
6 suppliers
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Haloxyfop-P

95977-29-0
63 suppliers
$36.70/25mg

References

Haloxyfop-P Related Search:

Fluroxypyr 2,4,6-Collidine Methyl 2-(4-((3-chloro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)propanoate 2-Chloro-5-(chloromethyl)pyridine 2-[4-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxyphenoxy]propanoic acid Diflufenican Methyltrimethoxysilane Epichlorohydrin 2,2-Bis(hydroxymethyl)propionic acid 2,6-Lutidine