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Structure of 1196157-14-8
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4-Bromo-5-methylpicolinaldehyde features a brominated pyridine core with a methyl substituent and aldehyde functionality, enabling direct incorporation into cross-coupling reactions. The electron-deficient heteroaryl ring facilitates palladium-catalyzed transformations, while the aldehyde group offers downstream derivatization potential. This bench-stable reagent streamlines access to complex nitrogen-containing scaffolds in medicinal chemistry and materials synthesis.
4-Bromo-5-methylpicolinaldehyde serves as a versatile building block in medicinal chemistry and cross-coupling synthesis. Its aldehyde functionality enables direct incorporation into imines, oximes, and reductive amination workflows, while the bromine atom facilitates palladium-catalyzed coupling reactions. The methyl group enhances lipophilicity and provides a handle for further functionalization. This compound exhibits good bench stability and is compatible with standard reaction conditions, making it suitable for iterative synthetic sequences in API development.
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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: