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Structure of 431046-15-0
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6-Chloro-1H-indol-4-amine features a chlorine-substituted indole core with a primary amine at the 4-position, enabling direct functionalization in C–H amination and cross-coupling reactions. The electron-deficient aromatic system enhances reactivity in palladium-catalyzed transformations, while the bench-stable nature supports handling under standard conditions. This scaffold serves as a key building block for bioactive heterocycles in medicinal chemistry.
6-Chloro-1H-indol-4-amine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C4 position of the indole scaffold. Its chloro substituent provides a handle for palladium-catalyzed cross-coupling reactions, while the primary amine facilitates derivatization via acylation or reductive amination. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthesis of bioactive heterocycles and targeted API intermediates.
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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: