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Structure of 1121051-30-6
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Ethyl 6-bromo-8-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate features a sterically hindered trifluoromethyl group and brominated imidazopyridine core, enabling direct functionalization in cross-coupling reactions. This bench-stable building block integrates seamlessly into pharmaceutical scaffolds requiring electron-deficient heterocyclic motifs.
Ethyl 6-bromo-8-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate serves as a versatile building block for constructing imidazo[1,2-a]pyridine-based scaffolds in medicinal chemistry. The bromine at C6 enables palladium-catalyzed cross-coupling reactions, while the trifluoromethyl group enhances metabolic stability and lipophilicity. The ester functionality offers handle for derivatization, and the molecule exhibits good bench stability and compatibility with standard synthetic protocols.
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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-H320-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: