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Structure of 950739-21-6
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3-Bromo-1H-pyrazol-5-amine features a bromine substituent at the 3-position and an amine group at the 5-position of the pyrazole ring, enabling direct functionalization in heterocyclic synthesis. This electron-deficient scaffold integrates readily into bioactive molecule design, offering high reactivity in palladium-catalyzed coupling reactions. The compound exhibits bench-stable handling under standard conditions and serves as a key intermediate in medicinal chemistry and materials science applications.
3-Bromo-1H-pyrazol-5-amine serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions to construct biologically relevant pyrazole derivatives. The bromo group facilitates efficient Suzuki, Stille, and Negishi couplings, while the primary amine offers direct functionalization potential. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for medicinal chemistry campaigns and API intermediate 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-H320-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: