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Structure of 945749-71-3
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This pyrimidine-based scaffold integrates a morpholinophenylamino group with a para-benzoic acid moiety, delivering enhanced solubility and metabolic stability. The electron-rich morpholine ring facilitates hydrogen bonding in kinase inhibition contexts, while the carboxylic acid enables conjugation or salt formation. Designed for targeted bioactive molecule development, this compound serves as a key intermediate in pharmaceutical discovery pipelines.
4-(2-(4-Morpholinophenylamino)pyrimidin-4-yl)benzoic acid serves as a versatile building block in medicinal chemistry, enabling the construction of kinase-inhibitor scaffolds. The pyrimidine core facilitates efficient coupling reactions, while the morpholinophenylamino moiety enhances solubility and modulates target affinity. Its carboxylic acid group allows for direct derivatization or salt formation, supporting purification and formulation. This compound exhibits bench stability and compatibility with standard synthetic workflows, making it a practical intermediate for drug discovery programs targeting oncology and inflammatory pathways.
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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: