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Structure of 1074-85-7
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(1H-Indol-4-yl)methanol features a benzene-fused indole core with a pendant hydroxymethyl group, delivering a versatile scaffold for synthetic modifications. This bench-stable derivative integrates readily into bioactive molecule design, where the polar methylene alcohol enhances solubility and serves as a handle for further functionalization.
(1H-Indol-4-yl)methanol serves as a versatile building block for indole-based scaffolds, enabling direct functionalization at the C4 position. Its aldehyde functionality facilitates reductive amination, Grignard additions, and coupling reactions with nucleophiles, while maintaining stability under standard bench conditions. The molecule functions effectively in the synthesis of heterocyclic libraries and bioactive compounds, offering straightforward purification and compatibility with common reaction protocols.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H318
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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: