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Structure of 171919-36-1
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1-Methyl-1H-pyrrolo[2,3-b]pyridine-3-carboxaldehyde delivers a rigid, electron-deficient heteroaromatic scaffold ideal for constructing bioactive molecules. The aldehyde functionality enables direct coupling in Ugi or Passerini reactions, while the methyl group enhances solubility and metabolic stability. This compound serves as a key building block in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active agents.
1-Methyl-1H-pyrrolo[2,3-b]pyridine-3-carboxaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient construction of nitrogen-containing heterocycles. Its aldehyde functionality facilitates reductive amination, Schiff base formation, and coupling reactions under mild conditions. The molecule exhibits good bench stability and compatibility with common functional groups, supporting its use in multi-step synthesis and library generation for drug discovery applications.
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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: