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Structure of 189281-66-1
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Methyl 2,6-dichloro-5-fluoronicotinate is a halogenated nicotinate ester featuring orthogonal substitution at the pyridine ring. This electron-deficient heterocycle integrates readily into synthetic sequences requiring precise steric and electronic control. The methyl ester group enables direct functionalization or hydrolysis to the corresponding acid under standard conditions. Bench-stable and moisture-tolerant, it serves as a robust building block in medicinal chemistry and agrochemical synthesis.
Methyl 2,6-dichloro-5-fluoronicotinate serves as a versatile building block in medicinal chemistry and agrochemical synthesis. Its electron-deficient pyridine core enables efficient Suzuki-Miyaura, Buchwald-Hartwig, and nucleophilic substitution reactions. The methyl ester group facilitates downstream derivatization, while the ortho-chloro and meta-fluoro substituents provide orthogonal reactivity for selective functionalization. Bench-stable and readily purified by flash chromatography, it functions as a key intermediate in the construction of heterocyclic scaffolds relevant to pharmaceutical development.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H410
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Precautionary Statements : P264-P273-P280-P302+P352-P362+P364-P391-P501
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Lot numbers can be found on the outside label of a product: