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Structure of 25742-00-1
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(3-Bromoisoxazol-5-yl)methanol features a brominated isoxazole ring fused to a primary alcohol, enabling direct functionalization in synthetic sequences. This bench-stable, moisture-tolerant heterocycle integrates readily into bioactive molecule scaffolds and serves as a key intermediate for medicinal chemistry campaigns requiring halogen-directed coupling or cyclization pathways.
(3-Bromoisoxazol-5-yl)methanol serves as a versatile building block for the synthesis of brominated heterocycles and bioactive molecules. Its isoxazole core provides structural rigidity and metabolic stability, while the pendant hydroxymethyl group enables facile derivatization via oxidation, etherification, or coupling reactions. The molecule exhibits excellent bench stability and compatibility with standard synthetic protocols, facilitating efficient incorporation into complex scaffolds for medicinal chemistry and process 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: