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Structure of 77556-44-6
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3-(4-Bromo-1H-pyrazol-1-yl)pyridine features a brominated pyrazole moiety linked to a pyridine ring, enabling efficient coupling in cross-coupling reactions. The electron-deficient pyridine and halogenated pyrazole provide complementary reactivity for transition metal-catalyzed transformations. This scaffold serves as a key building block in medicinal chemistry and materials science.
3-(4-Bromo-1H-pyrazol-1-yl)pyridine serves as a versatile building block for constructing bioactive heterocyclic scaffolds. The bromopyrazole moiety enables palladium-catalyzed cross-coupling reactions, while the pyridine ring offers orthogonal reactivity for further functionalization. Bench-stable and readily purified by column chromatography, it facilitates efficient synthesis of pharmaceutical intermediates and agrochemical candidates through established coupling protocols.
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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: