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Structure of 220844-76-8
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Methyl 7-bromoquinoline-4-carboxylate is a bench-stable, moisture-tolerant heterocyclic ester featuring a bromine atom at the C7 position and a methyl carboxylate group at C4. This electronic configuration enables efficient cross-coupling reactions, particularly in palladium-catalyzed transformations. The para-substituted quinoline scaffold provides enhanced solubility and stability under standard reaction conditions, facilitating integration into complex molecular architectures.
Methyl 7-bromoquinoline-4-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions at the C7 position. The quinoline scaffold provides inherent stability and π-conjugation, while the bromide facilitates functionalization via Suzuki, Stille, or Negishi couplings. The methyl ester group offers compatibility with standard reduction and hydrolysis protocols, allowing access to carboxylic acid derivatives. This compound exhibits excellent bench stability and is readily purified by flash chromatography, making it well-suited for iterative synthetic sequences in medicinal chemistry and materials science applications.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: