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Structure of 116855-03-9
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3-Bromo-1-methyl-1H-pyrazolo[3,4-b]pyridine features a brominated pyrazolopyridine core that enables direct functionalization in cross-coupling reactions. The methyl group enhances solubility and electronic modulation, while the bromine serves as a reactive handle for Pd-catalyzed transformations. This compound is bench-stable and well-suited for building complex heterocyclic architectures in medicinal chemistry and materials science.
3-Bromo-1-methyl-1H-pyrazolo[3,4-b]pyridine serves as a versatile building block for the synthesis of biologically active heterocycles. Its bromine atom enables palladium-catalyzed cross-coupling reactions, facilitating the construction of complex molecular architectures. The pyrazolopyridine core provides structural rigidity and favorable pharmacophore properties, while the methyl group enhances solubility and metabolic stability. This compound exhibits excellent bench stability and compatibility with standard synthetic protocols, making it well-suited for medicinal chemistry campaigns and process 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: