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Structure of 35251-99-1
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2,3-Dichloropyrido[3,4-b]pyrazine features a rigid, electron-deficient heteroaromatic core that facilitates selective coupling reactions in medicinal chemistry. This scaffold integrates readily into kinase inhibitors and other bioactive molecules, offering enhanced metabolic stability and favorable binding interactions within target protein pockets.
2,3-Dichloropyrido[3,4-b]pyrazine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the pyridine and pyrazine rings via palladium-catalyzed cross-coupling reactions. Its dichloro substitution pattern offers orthogonal reactivity for sequential derivatization, while maintaining bench stability and compatibility with standard synthetic workflows. The scaffold is well-suited for constructing complex heterocyclic architectures found in kinase inhibitors and other bioactive molecules.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: