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Structure of 915302-21-5
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2-Chloropyrido[3,2-d]pyrimidine delivers a reactive chloro substituent at the pyridine ring junction, enabling direct nucleophilic substitution under mild conditions. This electron-deficient heterocycle integrates readily into pharmaceutical scaffolds and serves as a key intermediate in kinase inhibitor development.
2-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 chloro group facilitates palladium-catalyzed cross-coupling reactions, while the fused pyridopyrimidine core provides structural rigidity and enhanced target binding affinity. Bench-stable and compatible with standard synthetic protocols, it functions reliably in multi-step synthesis and scale-up applications.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: