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Structure of 126807-09-8
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3-Bromo-6-nitro-1H-indole features a bromine atom at the 3-position and a nitro group at the 6-position on the indole core, creating a highly electron-deficient aromatic system. This configuration enables efficient cross-coupling reactions and facilitates functionalization in synthetic routes to bioactive heterocycles. The compound exhibits excellent stability under standard bench conditions and is compatible with palladium-catalyzed transformations.
3-Bromo-6-nitro-1H-indole serves as a versatile building block for the synthesis of functionalized indole scaffolds, enabling palladium-catalyzed cross-coupling reactions at the C3 position. The nitro group at C6 facilitates subsequent reduction and cyclization pathways, while the bromine moiety offers orthogonal reactivity for further diversification. Its bench-stable nature and compatibility with standard synthetic protocols make it well-suited for medicinal chemistry and materials science applications.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: