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Structure of 728034-12-6
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1H-Pyrrolo[2,3-b]pyridine-4-carboxaldehyde delivers a rigid, electron-deficient heteroaromatic scaffold ideal for constructing advanced pharmaceutical intermediates. The aldehyde functionality enables direct coupling in Ullmann or Buchwald-Hartwig reactions, while the fused pyrrolopyridine core enhances metabolic stability and target affinity in kinase inhibitor design.
1H-Pyrrolo[2,3-b]pyridine-4-carboxaldehyde serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its aldehyde functionality enables efficient derivatization via reductive amination, Wittig reactions, and coupling protocols. The scaffold exhibits excellent bench stability and compatibility with common protecting groups, facilitating modular synthesis of complex polycycles and bioactive molecules.
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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: