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Structure of 70555-46-3
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6-Methoxyindole-3-carboxaldehyde features a benzene-fused indole core with a methoxy group at the 6-position and a formyl substituent at C3. This electron-rich scaffold enables direct integration into heterocyclic synthesis, serving as a key building block for bioactive molecule design. The aldehyde functionality supports facile derivatization via nucleophilic addition or condensation reactions under standard conditions.
6-Methoxyindole-3-carboxaldehyde serves as a versatile building block in medicinal chemistry, enabling direct access to substituted indole scaffolds via classic condensation reactions. Its aldehyde functionality facilitates efficient imine formation and reductive amination, while the 6-methoxy group enhances solubility and modulates electronic properties. Bench-stable and compatible with standard purification protocols, it functions reliably in multistep syntheses requiring orthogonally protected heterocyclic intermediates.
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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: