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Structure of 53590-50-4
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5-Bromoindole-2-carboxaldehyde serves as a versatile building block for the synthesis of biologically relevant indole derivatives. Its aldehyde functionality enables efficient imine formation, Ugi reactions, and reductive amination, while the bromo group supports palladium-catalyzed cross-coupling transformations. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative medicinal chemistry campaigns and API intermediate development.
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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 : H319
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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: