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Structure of 35980-77-9
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2-Morpholinopyridin-4-amine features a pyridine core functionalized with a morpholine ring and a primary amine at the 4-position, enabling dual-site reactivity. This combination delivers enhanced solubility and tunable basicity, making it valuable for medicinal chemistry applications. The molecule integrates readily into kinase inhibitors and catalytic scaffolds due to its ability to engage in hydrogen bonding and coordinate metal centers.
2-Morpholinopyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to kinase inhibitors and other bioactive heterocycles. Its pyridine core provides a strong hydrogen bond acceptor site, while the morpholine ring enhances solubility and metabolic stability. The amine functionality facilitates straightforward derivatization via coupling reactions, and the molecule exhibits good bench stability and ease of purification—key attributes for scalable synthesis and high-throughput screening 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: