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Structure of 1174229-72-1
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Ethyl 2-(6-aminopyridin-3-yl)acetate features a pyridine core functionalized with an amino group at the 6-position and an acetyl ester side chain, enabling direct incorporation into heterocyclic scaffolds. This bench-stable intermediate supports efficient derivatization in medicinal chemistry campaigns targeting kinase inhibitors and bioactive nitrogen-containing compounds.
Ethyl 2-(6-aminopyridin-3-yl)acetate serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based pharmacophores. The pendant amino group facilitates direct derivatization via acylation, alkylation, or coupling reactions, while the ester functionality supports hydrolysis or transformation into amides and carboxylic acids. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for iterative synthesis of heterocyclic scaffolds relevant to kinase inhibitors and other bioactive molecules.
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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: