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Structure of 177360-11-1
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5-Bromo-6-methoxy-1H-indole features a brominated indole core with a methoxy group at the 6-position, enhancing solubility and electronic modulation. This bench-stable heterocycle integrates readily into synthetic routes for bioactive molecules, offering predictable reactivity in cross-coupling and functionalization processes.
5-Bromo-6-methoxy-1H-indole serves as a valuable building block for the synthesis of biologically active heterocycles and pharmaceutical intermediates. The bromo group enables palladium-catalyzed cross-coupling reactions, while the methoxy substituent provides electronic modulation and orthogonality in multi-step syntheses. This compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for scalable medicinal chemistry campaigns 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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: