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Structure of 850334-30-4
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4-Bromo-6-iodo-1H-indole features a uniquely functionalized indole core with bromo and iodo substituents at the 4- and 6-positions, respectively. This electron-deficient scaffold enables direct cross-coupling reactions under palladium catalysis, facilitating rapid access to complex heterocyclic architectures in medicinal chemistry and materials science. The molecule exhibits enhanced stability and predictable reactivity in standard synthetic workflows.
4-Bromo-6-iodo-1H-indole serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling the construction of biologically relevant indole scaffolds. Its complementary halogenation pattern supports sequential functionalization via orthogonal C–H activation or Suzuki-Miyaura coupling protocols. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for medicinal chemistry campaigns and process-scale synthesis.
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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: