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Structure of 1064678-14-3
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Methyl 4-bromo-2-chloronicotinate features a uniquely activated pyridine core bearing bromo and chloro substituents at the 4- and 2-positions, respectively. This electron-deficient heterocycle enables efficient cross-coupling reactions under palladium catalysis. The methyl ester group provides stability and facilitates downstream derivatization. This compound serves as a key intermediate in the synthesis of bioactive nitrogen-containing scaffolds.
Methyl 4-bromo-2-chloronicotinate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogenation pattern. The bromo and chloro substituents facilitate sequential functionalization under orthogonal conditions, while the methyl ester group supports subsequent transformations such as hydrolysis or reduction. Its bench-stable nature and compatibility with standard synthetic workflows make it ideal for constructing complex scaffolds in medicinal chemistry and agrochemical research.
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GHS Pictogram :
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GHS No : GHS08,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H361-H372-H410
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Precautionary Statements : P264-P280-P301+P330+P331
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Lot numbers can be found on the outside label of a product: