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Structure of 50735-34-7
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Methyl 2-amino-5-bromonicotinate features a brominated pyridine core with complementary amino and ester functionalities, enabling direct incorporation into heterocyclic scaffolds. The para-bromine facilitates palladium-catalyzed cross-coupling reactions, while the ortho-amino group offers nucleophilic reactivity for derivatization under mild conditions. This bench-stable intermediate supports efficient access to bioactive nitrogen heterocycles in medicinal chemistry campaigns.
Methyl 2-amino-5-bromonicotinate serves as a versatile building block in medicinal chemistry and synthetic organic chemistry. Its dual functionality—readily oxidizable amine and electrophilic bromide—enables sequential functionalization via Pd-catalyzed cross-coupling, nucleophilic substitution, and directed metalation. The methyl ester group facilitates derivatization or hydrolysis to the corresponding acid, while the ortho-amino and meta-bromo substituents provide orthogonal reactivity for scaffold diversification. This compound exhibits excellent bench stability and is compatible with standard purification techniques, making it ideal for high-throughput synthesis of heterocyclic libraries and API intermediates.
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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: