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Structure of 51108-29-3
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4-Fluoroisoindoline-1,3-dione serves as a reactive electrophilic scaffold for conjugate addition reactions, featuring a fluorine atom at the 4-position that enhances reactivity through inductive withdrawal. This electron-deficient heterocycle integrates readily into complex molecular architectures under mild conditions, offering high functional group tolerance and enabling efficient access to fluorinated analogs in synthetic organic chemistry workflows.
4-Fluoroisoindoline-1,3-dione serves as a versatile building block in medicinal chemistry, enabling efficient construction of bioactive heterocycles through nucleophilic substitution and cycloaddition reactions. Its fluorinated scaffold enhances metabolic stability and modulates electronic properties, while the diketone functionality offers robust compatibility with diverse functional groups. Bench-stable and readily purified, it facilitates scalable synthesis of pharmaceutical intermediates and API precursors.
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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: