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Structure of 1802489-57-1
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Methyl 1-amino-4-bromo-1H-pyrrole-2-carboxylate hydrochloride delivers a reactive bromo-pyrrole scaffold with enhanced solubility and stability. The amino group enables direct functionalization, while the methyl ester supports downstream derivatization. This bench-stable, moisture-tolerant reagent facilitates efficient access to complex heterocycles in medicinal chemistry and materials synthesis.
Methyl 1-amino-4-bromo-1H-pyrrole-2-carboxylate hydrochloride serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrroles via Pd-catalyzed cross-coupling and electrophilic substitution. The bromo group facilitates Suzuki, Stille, and Negishi couplings, while the protected amino and ester functionalities offer orthogonal reactivity for sequential transformations. Bench-stable and readily purified by recrystallization, it functions reliably in medicinal chemistry campaigns and API intermediate development.
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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-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: