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Structure of 3030-06-6
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1-Acetyl-5-bromo-4-chloro-1H-indol-3-yl acetate features a halogenated indole core with strategically positioned bromo and chloro substituents, enabling selective cross-coupling reactions. The acetyl group at the 1-position enhances solubility and stability, while the ester functionality at C3 supports downstream derivatization. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and pharmaceutical candidates.
1-Acetyl-5-bromo-4-chloro-1H-indol-3-yl acetate serves as a versatile building block for the synthesis of substituted indole derivatives, leveraging its orthogonal functionalization potential at C3 and C5 positions. The acetyl group at C1 enables direct electrophilic substitution or further derivatization, while the bromo and chloro substituents facilitate palladium-catalyzed cross-coupling reactions. Bench-stable and readily purified by flash chromatography, it functions effectively in late-stage diversification strategies for medicinal chemistry and heterocyclic scaffold 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 : 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: