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Structure of 92855-65-7
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7-(Benzyloxy)-1H-indole-3-carbaldehyde integrates a benzyl ether-stabilized indole scaffold with a reactive aldehyde handle, enabling direct coupling in C–H functionalization and heterocycle synthesis. This bench-stable derivative facilitates efficient access to biologically relevant indole alkaloid analogs under standard conditions.
7-(Benzyloxy)-1H-indole-3-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to indole-based scaffolds through standard coupling and functional group transformation protocols. The benzyloxy group provides orthogonal protection for phenolic hydroxyls, while the aldehyde functionality facilitates reductive amination, imine formation, and Mannich reactions. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for iterative synthesis 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: