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Structure of 1612287-20-3
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5-Bromo-2-chloro-1H-pyrrolo[2,3-b]pyridine features a fused heterocyclic core with strategically positioned halogens enabling direct functionalization in cross-coupling reactions. The electron-deficient pyrrolopyridine scaffold supports efficient Pd-catalyzed transformations, while the bromo and chloro substituents offer orthogonal reactivity for sequential derivatization. This bench-stable intermediate is well-suited for medicinal chemistry and materials synthesis.
5-Bromo-2-chloro-1H-pyrrolo[2,3-b]pyridine serves as a versatile heterocyclic building block for the synthesis of biologically active compounds and functional materials. Its dual halogenation pattern enables selective cross-coupling reactions, facilitating the construction of complex molecular architectures. The molecule exhibits excellent bench stability and compatibility with standard Pd-catalyzed transformations, simplifying purification and process scalability in medicinal chemistry and agrochemical research.
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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: