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Structure of 393553-55-4
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4-Bromo-6-methoxy-1H-indole features a bromine substituent at the 4-position and a methoxy group at the 6-position, conferring enhanced electronic modulation and improved solubility in organic media. This indole scaffold serves as a key building block for bioactive heterocycles, particularly in medicinal chemistry and agrochemical development.
4-Bromo-6-methoxy-1H-indole serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its well-defined electrophilic bromine site. The 6-methoxy group enhances solubility and modulates electronic properties, while the indole core provides a robust scaffold for heterocyclic diversification. Its bench-stable nature and compatibility with standard synthetic protocols facilitate efficient access to complex molecular architectures.
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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: