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Structure of 860757-84-2
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3-Bromoquinoline-6-carbaldehyde features a bromine substituent at the 3-position and an aldehyde group at the 6-position of the quinoline scaffold. This electron-deficient heterocycle integrates readily into cross-coupling reactions, serving as a key intermediate for bioactive molecule synthesis. The aldehyde functionality enables direct derivatization under mild conditions.
3-Bromoquinoline-6-carbaldehyde serves as a versatile building block in medicinal chemistry and catalytic synthesis, enabling direct functionalization at the quinoline core. The aldehyde group facilitates nucleophilic additions, reductive aminations, and coupling reactions, while the bromine substituent supports palladium-catalyzed cross-couplings such as Suzuki and Sonogashira transformations. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for constructing complex heterocyclic scaffolds 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: