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Structure of 36052-25-2
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Methyl 5-aminonicotinate features a pyridine ring bearing both an amino group at the 5-position and a methyl ester functionality. This electron-rich heterocycle serves as a key intermediate in the synthesis of bioactive compounds, particularly in medicinal chemistry and agrochemical development. The compound exhibits enhanced solubility and stability under standard conditions, enabling efficient derivatization through amide coupling or nucleophilic substitution reactions.
Methyl 5-aminonicotinate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted pyridine scaffolds. The ortho-amino and ester functionalities offer complementary reactivity for sequential functionalization—enabling electrophilic substitution, coupling reactions, and derivatization under mild conditions. Its bench-stable nature and straightforward purification make it well-suited for medicinal chemistry campaigns and process development workflows requiring nitrogen-rich heterocyclic motifs.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: