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Structure of 69627-03-8
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7-Chlorothieno[3,2-b]pyridine features a fused thienopyridine core with a chlorine substituent at the 7-position, conferring enhanced electron-deficiency and stability. This scaffold integrates readily into pharmaceutical intermediates and functional materials, offering predictable reactivity in cross-coupling and electrophilic substitution processes under standard conditions.
7-Chlorothieno[3,2-b]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and materials science applications. Its electron-deficient thienopyridine core enables efficient coupling reactions and facilitates functionalization at multiple positions. The chloro substituent provides a reliable handle for palladium-catalyzed cross-coupling transformations, enhancing synthetic accessibility in the development of bioactive compounds and advanced organic semiconductors.
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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: