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Structure of 1190321-59-5
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5-Bromo-6-chloro-1H-pyrrolo[2,3-b]pyridine is a heterocyclic building block featuring a bromo group at the 5-position and a chloro substituent at the 6-position on the pyrrolo[2,3-b]pyridine core. This electron-deficient scaffold enables direct functionalization in cross-coupling reactions, facilitating rapid access to complex nitrogen-containing architectures in medicinal chemistry and materials science.
5-Bromo-6-chloro-1H-pyrrolo[2,3-b]pyridine serves as a versatile building block for the synthesis of bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromo and chloro substituents facilitate sequential functionalization, while the pyrrolopyridine core provides a rigid scaffold suitable for medicinal chemistry exploration. Bench-stable and readily purified by column chromatography, it supports scalable synthesis in drug discovery workflows.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P405-P501
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Lot numbers can be found on the outside label of a product: