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Structure of 239097-74-6
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1,2-Benzoisoxazol-5-amine features a fused heterocyclic core with a primary amine at the 5-position, enabling direct functionalization in synthetic sequences. The electron-rich isoxazole ring enhances reactivity in coupling reactions, while the planar structure supports π-stacking interactions in molecular recognition applications. This bench-stable compound serves as a key scaffold for bioactive molecule design.
1,2-Benzoisoxazol-5-amine serves as a versatile heterocyclic building block in medicinal chemistry, enabling the synthesis of bioactive scaffolds through standard coupling and functionalization reactions. Its stability under ambient conditions and compatibility with common protecting group strategies facilitate efficient access to diverse analogs. The amine functionality allows direct incorporation into peptide-like architectures or further derivatization via acylation, alkylation, or transition-metal-catalyzed cross-coupling, making it a practical reagent for lead optimization campaigns.
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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: