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Structure of 1015460-62-4
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9-Bromo-5H-pyrido[4,3-b]indole features a brominated pyridoindole core with enhanced reactivity at the 9-position, enabling efficient cross-coupling transformations. This electron-deficient heterocycle serves as a key scaffold in medicinal chemistry for constructing complex nitrogen-containing architectures. The molecule exhibits excellent stability under standard handling conditions and integrates readily into synthetic sequences requiring halogen-functionalized building blocks.
9-Bromo-5H-pyrido[4,3-b]indole serves as a versatile building block for the synthesis of functionalized polycyclic scaffolds. The bromine substituent enables palladium-catalyzed cross-coupling reactions, facilitating efficient construction of biaryl and heteroaryl architectures. Its inherent stability under standard reaction conditions and compatibility with diverse functional groups make it well-suited for medicinal chemistry campaigns and API intermediate 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-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: