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Structure of 63762-72-1
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6-Chloro-5-methoxy-1H-indole features a chlorinated and methoxy-substituted indole core, offering enhanced electron-withdrawing character and improved solubility in organic media. This bench-stable heterocycle integrates readily into synthetic routes for pharmaceutical intermediates, enabling efficient construction of complex nitrogen-containing architectures under standard conditions.
6-Chloro-5-methoxy-1H-indole serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted indole scaffolds through palladium-catalyzed cross-coupling and electrophilic substitution reactions. Its orthogonal functionalization profile—combining a reactive chloro group with a stable methoxy substituent—facilitates sequential derivatization in medicinal chemistry and materials science applications. The compound exhibits excellent bench stability and simplifies purification in multi-step syntheses.
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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: