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Structure of 944086-09-3
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1-(7-Bromo-1H-indol-3-yl)ethanone features a brominated indole core paired with a ketone-functionalized ethyl side chain, enabling direct incorporation into bioactive scaffolds. This bench-stable compound serves as a key building block for medicinal chemistry campaigns targeting CNS modulators and kinase inhibitors.
1-(7-Bromo-1H-indol-3-yl)ethanone serves as a versatile building block for indole-based pharmaceutical intermediates. Its brominated indole core enables palladium-catalyzed cross-coupling reactions, while the acetyl group provides a handle for further functionalization via nucleophilic substitution or reduction. The compound exhibits good bench stability and facilitates efficient purification, making it well-suited for iterative synthesis in medicinal chemistry and API development workflows.
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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: