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Structure of 3034-53-5
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2-Bromothiazole was used to N-arylate 5- and 7-azaindoles. 2-Bromothiazole was also used as starting reagent in the synthesis of:2-cyanothiazole via cpper-catalyzed cyanation 2,4,5-trisubstituted thiazolesnovel electron-deficient fused pyrrolo[3,2-d:4,5-d]bisthiazole3-(2-thiazoyl)indoles
2-Bromothiazole serves as a versatile heterocyclic building block in synthetic organic chemistry, enabling direct functionalization at the thiazole ring via palladium-catalyzed cross-coupling reactions. Its bromine substituent facilitates Suzuki, Stille, and Negishi couplings with high efficiency and selectivity, making it valuable for constructing complex pharmaceutical scaffolds. The compound exhibits good bench stability and compatibility with common protecting groups, supporting its use in multi-step syntheses.
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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: