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Structure of 1952315-15-9
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3,5-Dichloropyrido[3,4-b]pyrazine features a rigid, electron-deficient heteroaromatic core that facilitates robust coupling reactions. This bifunctional scaffold integrates efficiently into medicinal chemistry libraries and serves as a key building block for kinase inhibitors and fluorescent probes under standard conditions.
3,5-Dichloropyrido[3,4-b]pyrazine serves as a versatile building block in medicinal chemistry, enabling the construction of heterocyclic scaffolds through palladium-catalyzed cross-coupling reactions. Its dichloro substitution pattern provides orthogonal reactivity for sequential functionalization, while its inherent stability facilitates handling and purification. The compound functions effectively in Suzuki-Miyaura and Buchwald-Hartwig coupling protocols, offering reliable access to complex nitrogen-containing architectures relevant to drug discovery.
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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: