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Structure of 1378865-57-6
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6'-Bromospiro[cyclopropane-1,3'-indolin]-2'-one features a rigid spirocyclic scaffold integrating a brominated cyclopropane with an indolinone core. This architecture imparts unique steric and electronic properties, enabling selective functionalization in synthetic sequences. The bromine atom serves as a high-reactivity handle for cross-coupling transformations, while the spiro configuration enhances structural rigidity and metabolic stability.
6'-Bromospiro[cyclopropane-1,3'-indolin]-2'-one serves as a versatile building block for the synthesis of spirocyclic indoline scaffolds prevalent in medicinal chemistry. The bromine at the 6' position enables palladium-catalyzed cross-coupling reactions, facilitating C–C bond formation under mild conditions. Its spirocyclic architecture confers rigidity and enhanced metabolic stability, while the ketone functionality offers opportunities for derivatization via nucleophilic addition or enolization. Bench-stable and readily purified by column chromatography, it functions effectively in multi-step syntheses of complex heterocycles and 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-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: