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Structure of 936092-87-4
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4-Bromo-7-methyl-1H-indole features a sterically accessible indole core with complementary halogen and methyl substituents, enabling direct functionalization in cross-coupling and electrophilic substitution reactions. The bromine atom serves as a high-reactivity handle for palladium-catalyzed transformations, while the methyl group enhances electron density at the C7 position, improving stability and solubility under standard conditions.
4-Bromo-7-methyl-1H-indole serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions for C–C bond formation. Its bromine substituent provides high reactivity in Suzuki, Stille, and Negishi couplings, while the methyl group enhances solubility and modulates electronic properties. The indole core offers robust stability under standard synthetic conditions, facilitating efficient functionalization and purification.
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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: