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Structure of 342613-67-6
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3-Bromo-7-chloroimidazo[1,2-a]pyridine is a heterocyclic scaffold featuring complementary halogen substituents at positions 3 and 7. This electron-deficient core enables direct coupling in cross-coupling reactions and facilitates integration into bioactive molecules. The molecule exhibits robust stability under standard reaction conditions and serves as a key intermediate in medicinal chemistry and materials science applications.
3-Bromo-7-chloroimidazo[1,2-a]pyridine serves as a versatile building block for constructing bioactive heterocycles in medicinal chemistry. The molecule enables palladium-catalyzed cross-coupling reactions due to its bromo substituent, while the chloro group offers orthogonal reactivity. Its stability under standard synthetic conditions and compatibility with diverse functional groups facilitate efficient assembly of complex scaffolds, making it valuable for drug discovery campaigns requiring modular imidazopyridine frameworks.
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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: