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Structure of 63754-96-1
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6-Fluoro-2(3H)-benzothiazolone features a fluorinated benzothiazolone core with enhanced electron-withdrawing character, enabling efficient coupling in cross-coupling and heterocycle functionalization. This bench-stable scaffold integrates readily into bioactive molecule synthesis, offering improved metabolic stability and membrane permeability for medicinal chemistry applications.
6-Fluoro-2(3H)-benzothiazolone serves as a versatile building block for heterocyclic synthesis, offering enhanced reactivity at the C6 position due to the electron-withdrawing fluorine substituent. It functions as a key scaffold in medicinal chemistry and materials science, enabling efficient functionalization via nucleophilic substitution or palladium-catalyzed coupling. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic workflows in API development and advanced intermediate construction.
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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: