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Structure of 849067-97-6
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1H-Pyrrolo[2,3-b]pyridin-5-ylmethanol offers a rigid heteroaromatic scaffold with a pendant hydroxymethyl group, enabling direct functionalization or conjugation in synthetic routes. This bench-stable building block integrates readily into bioactive molecule frameworks, particularly in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
1H-Pyrrolo[2,3-b]pyridin-5-ylmethanol serves as a versatile building block for heterocyclic synthesis, enabling efficient functionalization at the benzylic position. Its stability under standard reaction conditions and compatibility with diverse coupling and oxidation protocols facilitate access to complex scaffolds relevant in medicinal chemistry. The molecule functions effectively as a key intermediate in the construction of bioactive pyrrolopyridine derivatives.
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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: