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Structure of 879132-46-4
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This pyrrolopyridine derivative features a silyl-protected alcohol moiety enabling stable storage and selective deprotection under mild conditions. The trimethylsilyl group enhances solubility and compatibility in synthetic workflows, while the fused heterocyclic core provides a rigid scaffold for C–H functionalization and transition-metal-catalyzed coupling reactions.
1-((2-(Trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine serves as a robust building block for heterocyclic synthesis, enabling efficient access to pyrrolopyridine-based scaffolds. The trimethylsilyl ether group provides excellent bench stability and facilitates orthogonal deprotection under mild conditions. It functions effectively in palladium-catalyzed coupling reactions and supports diverse functionalization strategies in medicinal chemistry 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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: