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Structure of 33515-62-7
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4-Iodopyrrole-2-carboxaldehyde features a reactive aldehyde group flanked by an iodine atom at the C4 position, enabling direct functionalization in cross-coupling and conjugation workflows. This bench-stable heterocycle integrates readily into complex molecular architectures, offering precise control over electronic and steric profiles in synthetic applications.
4-Iodopyrrole-2-carboxaldehyde serves as a versatile building block for constructing biologically relevant heterocycles and pharmaceutical scaffolds. The aldehyde functionality enables direct coupling in Ullmann-type reactions, Suzuki-Miyaura cross-couplings, and reductive amination protocols. Its iodine handle facilitates palladium-catalyzed transformations, while the pyrrole core provides inherent π-electron richness suitable for further functionalization. Bench-stable and compatible with standard purification techniques, it functions effectively in multi-step synthesis workflows targeting complex molecular architectures.
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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: