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Structure of 2567498-97-7
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2,5-Dichlorothiazolo[4,5-b]pyridine features a fused heterocyclic core combining thiazole and pyridine rings, bearing chlorine substituents at key positions for enhanced reactivity. This electron-deficient scaffold integrates readily into synthetic sequences requiring polarizable, planar platforms. The molecule exhibits bench-stable handling characteristics and serves as a strategic building block in the development of functionalized heteroaromatic systems.
2,5-Dichlorothiazolo[4,5-b]pyridine serves as a versatile heterocyclic building block in medicinal chemistry, enabling the construction of complex scaffolds through palladium-catalyzed cross-coupling reactions. Its electrophilic chloride substituents facilitate efficient functionalization under mild conditions, while the fused thiazole-pyridine core provides enhanced metabolic stability and favorable binding interactions. The compound exhibits excellent bench stability and compatibility with diverse functional groups, making it a practical choice for lead optimization and API synthesis.
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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: