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Structure of 885523-35-3
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Methyl 7-bromo-1H-indole-5-carboxylate features a brominated indole core with a methyl ester at the 5-position, enabling direct incorporation into diverse synthetic scaffolds. The electron-deficient aromatic system enhances reactivity in transition-metal-catalyzed couplings, while the bench-stable ester group simplifies handling and purification under standard conditions.
Methyl 7-bromo-1H-indole-5-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized indole scaffolds. The bromine at the C7 position facilitates palladium-catalyzed cross-coupling reactions, while the ester group offers compatibility with reduction, hydrolysis, and further derivatization. This compound exhibits excellent bench stability and is well-suited for use in medicinal chemistry campaigns targeting heterocyclic APIs.
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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: