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Structure of 107818-55-3
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Methyl 3-amino-5-bromothiophene-2-carboxylate features a brominated thiophene core with complementary amino and ester functionalities, enabling direct integration into cross-coupling and cyclization sequences. This bench-stable heterocycle serves as a key intermediate for bioactive molecule synthesis, particularly in medicinal chemistry and agrochemical development.
Methyl 3-amino-5-bromothiophene-2-carboxylate serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted thiophene scaffolds via Pd-catalyzed cross-coupling and electrophilic functionalization. The amino and bromo groups offer orthogonal reactivity for sequential derivatization, while the ester functionality supports further manipulation. Bench-stable and readily purified by chromatography, it facilitates streamlined synthesis of bioactive intermediates in medicinal chemistry and materials science applications.
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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: