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Structure of 1204298-52-1
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4-Bromo-6-methylisoquinoline delivers a sterically accessible isoquinoline core with complementary halogen and methyl handles. This bench-stable scaffold integrates readily into cross-coupling workflows, enabling rapid access to functionalized heterocycles for medicinal chemistry and materials applications.
4-Bromo-6-methylisoquinoline serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions for the construction of complex isoquinoline-based scaffolds. Its bromine handle facilitates reliable C–C bond formation under standard Suzuki, Stille, or Negishi conditions, while the methyl group enhances electronic and steric control. The compound exhibits good bench stability and is compatible with a range of functional groups, making it ideal for iterative synthesis of bioactive heterocycles.
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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: