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Structure of 723-89-7
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1-Phenylindoline-2,3-dione features a fused tricyclic core with a quinone moiety that enables participation in redox-active transformations. This electron-deficient scaffold integrates readily into synthetic sequences requiring stable, planar heterocyclic intermediates. The phenyl substituent enhances rigidity and facilitates π-stacking interactions in supramolecular applications.
1-Phenylindoline-2,3-dione serves as a versatile building block in synthetic organic chemistry, enabling efficient access to complex heterocyclic scaffolds. Its fused indoline-dione framework exhibits robust bench stability and tolerates a range of functional groups, facilitating downstream transformations such as reductive cleavage, nucleophilic substitution, and cycloaddition reactions. This compound functions as a key intermediate in the construction of biologically relevant frameworks, particularly in medicinal chemistry campaigns targeting kinase inhibitors and other bioactive molecules.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: