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Structure of 1060805-64-2
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4-Bromo-6-chloropyridine-3-carbaldehyde features a pyridine core functionalized with bromo, chloro, and formyl groups at distinct positions, enabling selective coupling in cross-coupling and heterocyclic synthesis. The electron-deficient aromatic ring enhances reactivity in nucleophilic substitution, while the aldehyde group provides a handle for imine formation or derivatization. This compound serves as a key intermediate in pharmaceutical and agrochemical research.
4-Bromo-6-chloropyridine-3-carbaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct incorporation of halogenated pyridine scaffolds into target molecules. The aldehyde functionality facilitates nucleophilic additions, reductive aminations, and condensation reactions, while the bromo and chloro substituents support subsequent cross-coupling transformations such as Suzuki-Miyaura and Stille reactions. Bench-stable and compatible with standard purification methods, it functions effectively in multi-step syntheses requiring orthogonal reactivity.
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GHS Pictogram :
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GHS No : GHS07
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: