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Structure of 23351-05-5
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4-(1H-Pyrrol-1-yl)benzaldehyde integrates a pyrrole ring directly conjugated to an aromatic aldehyde, enabling efficient coupling in transition-metal-catalyzed transformations. This electron-rich scaffold facilitates C–C bond formation under mild conditions, offering high functional group tolerance and stability during synthesis of bioactive heterocycles and fluorescent probes.
4-(1H-Pyrrol-1-yl)benzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling the construction of biologically relevant heterocyclic scaffolds. Its conjugated aldehyde functionality facilitates efficient imine formation and reductive amination, while the pyrrole ring provides a robust platform for electrophilic substitution and transition-metal-catalyzed coupling reactions. The compound exhibits good bench stability and is compatible with common protecting group strategies, making it well-suited for iterative synthesis in medicinal chemistry and materials science 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: