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Structure of 151509-01-2
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Methyl 2-(aminomethyl)nicotinate hydrochloride features a pyridine ring bearing both an ester and a primary amine functionality, enabling direct derivatization in peptide and heterocyclic synthesis. The protonated amine enhances solubility in aqueous systems while maintaining stability under standard bench conditions. This salt form facilitates handling and incorporation into medicinal chemistry campaigns targeting nicotinamide analogs.
Methyl 2-(aminomethyl)nicotinate hydrochloride serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive pyridine derivatives. The pendant aminomethyl group facilitates direct functionalization, including reductive amination and amidation, while the methyl ester supports orthogonal transformations. Its crystalline form and bench-stable hydrochloride salt ensure ease of handling and purification, making it well-suited for iterative synthesis and API development workflows.
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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: