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Structure of 175358-02-8
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4,6-Dichloropyrido[3,2-d]pyrimidine serves as a pivotal heterocyclic scaffold in medicinal chemistry, featuring two chlorine substituents that enable selective functionalization at C4 and C6 positions. This electron-deficient core integrates readily into kinase inhibitors and antiviral agents, offering enhanced binding affinity through halogen bonding interactions. The compound exhibits bench-stable handling characteristics and compatibility with standard cross-coupling protocols under inert conditions.
4,6-Dichloropyrido[3,2-d]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of purine-based scaffolds. The dichloro substitution pattern facilitates selective Suzuki-Miyaura and Buchwald-Hartwig couplings, offering reliable access to functionalized heterocycles. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for iterative synthesis workflows in drug discovery and API development.
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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: