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Structure of 1000341-00-3
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6-Bromo-4-fluoroindolin-2-one features a fused indolinone scaffold with strategic halogenation at the 6-position and fluorine at the 4-position. This electron-deficient core enables direct functionalization in cross-coupling reactions and serves as a key building block for bioactive heterocycles in medicinal chemistry.
6-Bromo-4-fluoroindolin-2-one serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling efficient access to substituted indolines via palladium-catalyzed cross-coupling. The ortho-halogenation pattern facilitates selective functionalization, while the fluoro substituent enhances metabolic stability and modulates electronic properties. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for scalable synthesis of bioactive scaffolds.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: