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Structure of 1219741-50-0
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6-Bromo-3-methyl-1H-indole delivers a sterically accessible indole scaffold with complementary halogen and alkyl functionalities. This bench-stable heterocycle integrates readily into cross-coupling protocols, enabling direct access to substituted indole architectures in medicinal chemistry and materials synthesis.
6-Bromo-3-methyl-1H-indole serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling direct functionalization at the C2 position via palladium-catalyzed cross-coupling. The bromine and methyl groups offer orthogonal reactivity for sequential modifications, while the indole core provides inherent stability and compatibility with standard reaction conditions. Its bench-stable crystalline form facilitates handling and purification, making it ideal for scalable synthesis of biologically active scaffolds and API intermediates.
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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: