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Structure of 6188-43-8
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Imidazo[1,2-a]pyridine-3-carbaldehyde features a rigid heteroaromatic core with a reactive aldehyde group at the 3-position. This scaffold integrates seamlessly into bioactive molecule design, offering enhanced metabolic stability and favorable binding interactions in target-directed synthesis. The aldehyde moiety enables efficient coupling reactions for diversification in medicinal chemistry campaigns.
Imidazo[1,2-a]pyridine-3-carbaldehyde serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its aldehyde functionality enables efficient derivatization via reductive amination, Grignard additions, and Wittig reactions. The scaffold exhibits robust bench stability and compatibility with common protecting group strategies, facilitating modular synthesis of complex molecular architectures.
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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: