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Structure of 324-03-8
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6-Fluoro-1H-indole-2,3-dione features a fluorinated indole core with dual carbonyl groups, delivering enhanced electron-withdrawing character and improved metabolic stability. This scaffold integrates readily into synthetic routes for bioactive molecules, particularly in medicinal chemistry applications requiring halogenated heterocyclic motifs.
6-Fluoro-1H-indole-2,3-dione serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated heterocyclic scaffolds. Its reactive quinone core facilitates nucleophilic addition and cycloaddition reactions, while the fluorine substituent enhances metabolic stability and modulates electronic properties. The compound exhibits excellent bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis workflows in API 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: