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Structure of 1201633-72-8
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2-Bromo-5,6-dihydrobenzo[d]thiazol-7(4H)-one features a brominated dihydrothiazole core with a lactam functionality, offering a reactive handle for nucleophilic substitution and transition metal-catalyzed coupling. The electron-deficient heterocycle facilitates conjugation in synthetic intermediates, enabling efficient integration into bioactive scaffolds under standard conditions.
2-Bromo-5,6-dihydrobenzo[d]thiazol-7(4H)-one serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted benzo[d]thiazole scaffolds. Its bromine substituent facilitates palladium-catalyzed coupling reactions, while the enaminone functionality supports nucleophilic additions and cyclizations. The compound exhibits good bench stability and is compatible with standard purification methods, making it suitable for iterative synthesis in medicinal chemistry and process development workflows.
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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: