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Structure of 879132-48-6
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This pyrrolopyridinone derivative features a strategically positioned (trimethylsilyl)ethoxy methyl group that enhances solubility and stability during synthesis. The silyl-protected alcohol facilitates controlled deprotection, enabling seamless integration into complex molecular architectures. Ideal for medicinal chemistry campaigns requiring robust, functionalized heterocyclic scaffolds.
1-((2-(Trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridin-2(3H)-one serves as a versatile building block for the synthesis of pyrrolopyridine-based scaffolds, offering enhanced stability and orthogonal protection. The trimethylsilyl ether functionality enables reliable deprotection under mild conditions, facilitating downstream functionalization. Its compatibility with standard coupling reactions and robust bench stability make it well-suited for medicinal chemistry campaigns and process development workflows.
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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: