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Structure of 1075-26-9
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(1H-Indol-6-yl)methanol features a benzene-fused indole core with a reactive primary alcohol at the 6-position, enabling straightforward functionalization. This bench-stable, moisture-tolerant scaffold integrates readily into synthetic routes for bioactive molecules and fluorescent probes.
(1H-Indol-6-yl)methanol serves as a versatile building block for indole-based scaffolds, enabling efficient functionalization at the 6-position. Its benzylic alcohol functionality facilitates oxidation to aldehydes or carboxylic acids, and it participates reliably in Mitsunobu reactions, ether formation, and coupling protocols. The compound exhibits good bench stability and is compatible with common protecting group strategies, making it well-suited for medicinal chemistry campaigns and heterocycle synthesis.
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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: