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Structure of 886371-10-4
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Methyl 2-amino-5-methylnicotinate features a pyridine core bearing an amino group at C2 and a methyl substituent at C5, enabling direct functionalization in heterocyclic synthesis. The ester handle facilitates derivatization under standard conditions, while the electron-rich nitrogen enhances reactivity in cross-coupling and metal-mediated transformations. This bench-stable intermediate supports rapid access to bioactive analogs in medicinal chemistry workflows.
Methyl 2-amino-5-methylnicotinate serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted nicotinamide derivatives and heterocyclic scaffolds. Its amino and ester functionalities offer orthogonal reactivity for selective transformations, while the methyl group enhances metabolic stability. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for multi-step synthesis and scale-up 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: