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Structure of 1357945-38-0
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3-Bromo-4-chloro-1H-pyrazolo[3,4-b]pyridine features a fused bicyclic core with complementary halogen substituents enabling diverse cross-coupling transformations. The bromine and chlorine atoms facilitate selective functionalization in palladium-catalyzed reactions, while the electron-deficient pyridine ring enhances reactivity in nucleophilic substitution processes. This scaffold delivers access to complex heterocyclic architectures under standard conditions.
3-Bromo-4-chloro-1H-pyrazolo[3,4-b]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its dual halogenation enables efficient Pd-catalyzed cross-coupling reactions, including Suzuki-Miyaura and Buchwald-Hartwig aminations, with excellent functional group tolerance. The molecule exhibits robust bench stability and facilitates the construction of complex polycyclic scaffolds commonly found in kinase inhibitors and bioactive small molecules.
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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-H312-H315-H319-H332-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: