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Structure of 62226-17-9
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4-Chlorothieno[2,3-b]pyridine features a fused thienopyridine core with a chlorine substituent at the 4-position, delivering enhanced electron-deficiency and improved stability for use in cross-coupling reactions. This heterocyclic scaffold integrates readily into bioactive molecules and functional materials, offering predictable reactivity under standard conditions.
4-Chlorothieno[2,3-b]pyridine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient construction of fused thienopyridine scaffolds. Its chlorine substituent facilitates palladium-catalyzed cross-coupling reactions, while the electron-deficient core exhibits favorable reactivity in nucleophilic substitution and C–H functionalization processes. The compound demonstrates excellent bench stability and compatibility with standard purification techniques, making it well-suited for scalable synthesis and structure-activity studies.
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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: