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Structure of 700-85-6
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5-Fluoroisobenzofuran-1(3H)-one features a fused bicyclic core with a fluorine atom at the 5-position, imparting enhanced electron-withdrawing character and metabolic stability. This moiety integrates readily into bioactive scaffolds, offering improved lipophilicity and target engagement in medicinal chemistry applications.
5-Fluoroisobenzofuran-1(3H)-one serves as a versatile building block in synthetic organic chemistry, enabling efficient access to fluorinated heterocyclic scaffolds. Its inherent reactivity facilitates nucleophilic addition and transition-metal-catalyzed coupling reactions, while the fluoro substituent enhances metabolic stability and modulates electronic properties. The compound exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for medicinal chemistry campaigns 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: