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Structure of 61545-41-3
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6-Methyl-1H-indol-4-ol features a sterically accessible indole core with a hydroxyl group at C4 and a methyl substituent at C6, enabling direct functionalization in late-stage synthesis. The phenolic moiety enhances solubility and facilitates hydrogen bonding in catalytic systems. This bench-stable scaffold supports diverse applications in medicinal chemistry and materials science.
6-Methyl-1H-indol-4-ol serves as a versatile building block for indole-based scaffolds in medicinal chemistry and materials science. Its phenolic hydroxyl group enables direct functionalization, while the methyl substituent enhances metabolic stability and modulates electronic properties. The compound exhibits good bench stability and facilitates coupling reactions with minimal purification challenges, making it suitable for use in standard cross-coupling, cyclization, and derivatization protocols common in API development.
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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: