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Structure of 1060802-23-4
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5-Bromo-2-chloroisonicotinaldehyde features a highly reactive aldehyde group flanked by bromo and chloro substituents at the 5- and 2-positions of the pyridine ring. This electron-deficient scaffold enables direct incorporation into cross-coupling reactions, offering precise control over regiochemistry in synthetic sequences. The compound demonstrates stability under standard handling conditions and serves as a key building block for functionalized heterocycles.
5-Bromo-2-chloroisonicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling direct incorporation of halogenated pyridine motifs into target molecules. Its aldehyde functionality facilitates nucleophilic addition and condensation reactions, while the ortho-halogen substituents support palladium-catalyzed cross-coupling transformations. The compound exhibits good bench stability and is compatible with standard protecting group strategies, making it well-suited for modular synthesis of functionalized heterocycles and API intermediates.
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: