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Structure of 25369-33-9
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7-Chloroindolin-2-one is a bench-stable heterocyclic scaffold featuring a chlorinated indolinone core, offering enhanced electron-withdrawing character and improved solubility in polar organic solvents. This structural motif serves as a key building block in medicinal chemistry, enabling efficient incorporation into kinase inhibitors and bioactive molecules through direct functionalization at the C3 position.
7-Chloroindolin-2-one serves as a versatile building block in medicinal chemistry, enabling efficient access to indole-based scaffolds through standard functional group transformations. Its bench-stable nature and compatibility with diverse coupling reactions facilitate straightforward incorporation into complex molecules. The chloro substituent enhances electrophilic reactivity at the C7 position, supporting further derivatization in key synthetic sequences. This compound functions effectively in the construction of kinase inhibitors and other bioactive heterocycles.
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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-H412
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Precautionary Statements : P264-P270-P273-P330-P501
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Lot numbers can be found on the outside label of a product: