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Structure of 3139-10-4
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5-Methoxy-6-methyl-1H-indole features a fused bicyclic core with complementary electron-donating substituents: a methoxy group at C5 and a methyl group at C6. This combination enhances electron density across the indole ring, promoting reactivity in electrophilic substitution and facilitating incorporation into functionalized heterocycles for medicinal chemistry applications. The molecule exhibits bench-stable handling characteristics under standard conditions.
5-Methoxy-6-methyl-1H-indole serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to indole-based scaffolds through standard electrophilic substitution and transition-metal-catalyzed coupling reactions. Its ortho-substituted framework provides enhanced stability and predictable regioselectivity, facilitating downstream derivatization. The molecule exhibits excellent bench stability and is compatible with common purification methods, making it well-suited for high-throughput synthesis and process development workflows.
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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: