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Structure of 3335-98-6
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1-Phenyloxindole features a fused oxindole core with a phenyl substituent at the 1-position, delivering enhanced stability and tunable electronic properties. This scaffold integrates readily into medicinal chemistry campaigns targeting kinase inhibition and protein-protein interactions. The planar, electron-rich architecture supports efficient π-stacking in biological binding pockets.
1-Phenyloxindole serves as a versatile building block in medicinal chemistry, enabling the construction of biologically relevant heterocyclic scaffolds. Its oxindole core exhibits inherent stability and favorable functional group tolerance, facilitating downstream derivatization via C3 alkylation, N-arylation, or palladium-catalyzed coupling reactions. The phenyl substituent enhances π-stacking potential and modulates electronic properties, supporting its use in target-oriented synthesis.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: