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Structure of 86915-22-2
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7-Bromo-3-methyl-1H-indole features a brominated indole core with a methyl group at the 3-position, offering enhanced electron deficiency and improved stability under standard conditions. This scaffold serves as a key building block in medicinal chemistry, enabling direct incorporation into bioactive molecules via cross-coupling reactions.
7-Bromo-3-methyl-1H-indole serves as a versatile building block for the synthesis of biologically active heterocycles, particularly in medicinal chemistry and agrochemical development. The bromine at C7 enables palladium-catalyzed cross-coupling reactions, while the methyl group at C3 provides a site for selective functionalization. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient access to complex indole scaffolds used in API discovery.
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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: