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Structure of 51674-77-2
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4-Chloropyrido[3,2-d]pyrimidine serves as a pivotal heterocyclic scaffold in medicinal chemistry, featuring a chlorine atom at the 4-position that enables direct functionalization. This electron-deficient system integrates readily into kinase inhibitors and other bioactive molecules, offering high reactivity under standard coupling conditions.
4-Chloropyrido[3,2-d]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of kinase inhibitors and other bioactive heterocycles. Its chlorine substituent facilitates palladium-catalyzed cross-coupling reactions, while the fused pyridopyrimidine core offers enhanced metabolic stability and predictable binding interactions. The compound exhibits excellent bench stability and compatibility with common protecting group strategies, facilitating straightforward purification and integration into multi-step synthetic sequences.
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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: