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Structure of 1234616-70-6
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6-Bromo-2,4-dichloropyrido[2,3-d]pyrimidine features a rigid heteroaromatic core with strategically positioned halogens enabling direct functionalization. The bromine at the 6-position facilitates palladium-catalyzed cross-coupling, while the 2,4-dichloro substitution provides orthogonal reactivity for sequential derivatization. This compound serves as a high-impact scaffold in kinase inhibitor development and advanced medicinal chemistry campaigns.
6-Bromo-2,4-dichloropyrido[2,3-d]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromine and two chloro groups provide orthogonal reactivity for sequential derivatization, while the pyridopyrimidine core offers structural rigidity and favorable electronic properties for target engagement. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for high-throughput synthesis of kinase inhibitors and other bioactive heterocycles.
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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: