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Structure of 1780-72-9
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4-Bromo-5-methyl-1H-pyrazol-3-amine features a bromine substituent at C4 and a methyl group at C5, creating a sterically hindered, electron-deficient pyrazole core. This scaffold integrates readily into heterocyclic frameworks, enabling efficient coupling in medicinal chemistry applications. The primary amine facilitates conjugation and functionalization under standard conditions.
4-Bromo-5-methyl-1H-pyrazol-3-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyrazole scaffolds. Its bromo group facilitates palladium-catalyzed cross-coupling reactions, while the primary amine supports derivatization via acylation or condensation. The methyl substituent enhances metabolic stability and modulates electronic properties. Bench-stable and readily purified by recrystallization, it functions effectively in standard synthetic workflows for targeted heterocycle elaboration.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: