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Structure of 936011-17-5
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5-Bromo-2-methoxyisonicotinaldehyde delivers a trifunctional scaffold featuring a bromo group, methoxy substituent, and aldehyde handle at the pyridine ring. This electron-deficient heterocycle enables direct coupling in cross-coupling reactions, while the aldehyde facilitates conjugation via nucleophilic addition or oxime formation. The molecule exhibits bench-stable handling characteristics and compatibility with standard synthetic protocols.
5-Bromo-2-methoxyisonicotinaldehyde serves as a versatile building block in synthetic medicinal chemistry, enabling direct incorporation of bromo and methoxy groups into heterocyclic scaffolds. Its aldehyde functionality facilitates reductive amination, Grignard additions, and coupling reactions with nucleophiles. The compound exhibits good bench stability and is compatible with standard protecting group strategies, making it suitable for modular synthesis of bioactive molecules and API intermediates.
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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: