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Structure of 189628-37-3
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5-Bromo-2-chlorobenzaldehyde features a strategically positioned aldehyde group flanked by bromo and chloro substituents, enabling direct incorporation into cross-coupling reactions. This electron-deficient aromatic scaffold offers enhanced reactivity in palladium-catalyzed transformations and provides a robust platform for synthesizing complex pharmaceutical intermediates under standard conditions.
5-Bromo-2-chlorobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The aldehyde functionality facilitates downstream transformations such as reductive amination and Wittig reactions, while the bromo and chloro substituents offer complementary sites for sequential functionalization. Bench-stable and readily purified by distillation or chromatography, it functions reliably in multi-step syntheses requiring precise regiocontrol.
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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: