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Structure of 1065100-83-5
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(1H-Pyrrolo[2,3-b]pyridin-3-yl)methanol features a heteroaromatic core with a pendant hydroxymethyl group, enabling direct functionalization in late-stage synthesis. This bench-stable scaffold integrates readily into bioactive molecules, offering enhanced solubility and metabolic stability in pharmaceutical development workflows.
(1H-Pyrrolo[2,3-b]pyridin-3-yl)methanol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to pharmacologically relevant scaffolds. The pendant alcohol functions as a handle for derivatization via oxidation, protection, or coupling reactions, while the fused pyrrolopyridine core exhibits favorable stability and compatibility with common reaction conditions. Its utility in medicinal chemistry workflows is supported by predictable reactivity and straightforward purification.
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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: