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Structure of 1214336-33-0
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Methyl 2-bromo-5-chloroisonicotinate is a bench-stable, electron-deficient heterocyclic ester featuring orthogonal halogen handles at the 2- and 5-positions. This structural motif enables selective cross-coupling reactions in synthetic sequences, particularly in late-stage functionalization of bioactive scaffolds. The methyl ester group supports direct derivatization or hydrolysis to the corresponding acid.
Methyl 2-bromo-5-chloroisonicotinate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromine at the 2-position facilitates efficient Suzuki, Stille, or Negishi coupling, while the chlorine at the 5-position remains inert under standard conditions, allowing for sequential functionalization. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for medicinal chemistry campaigns and API intermediate development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P405-P501
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Lot numbers can be found on the outside label of a product: