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Structure of 192189-18-7
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This 1H-Pyrrolo[2,3-b]pyridine-1-carboxylic acid derivative features a sterically shielded tert-butyl ester group that enhances stability and simplifies purification. The 3-iodo substituent provides a reactive handle for downstream functionalization via cross-coupling, enabling efficient access to complex heterocyclic architectures in medicinal chemistry and materials science.
The 1,1-dimethylethyl ester of 3-iodo-1H-pyrrolo[2,3-b]pyridine-1-carboxylic acid serves as a stable, bench-ready building block for late-stage functionalization in heterocyclic synthesis. Its iodide moiety enables reliable Suzuki-Miyaura and Sonogashira coupling reactions, while the ester group offers orthogonal reactivity and ease of purification. This compound functions effectively in constructing complex scaffolds relevant to medicinal chemistry and materials science.
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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: