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Structure of 23876-39-3
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4,7-Dimethoxy-1H-indole features two methoxy groups at the 4- and 7-positions of the indole core, enhancing solubility and electronic donation. This electron-rich scaffold serves as a stable building block in synthetic organic chemistry, particularly for pharmaceutical intermediates and functional materials.
4,7-Dimethoxy-1H-indole serves as a valuable building block in medicinal chemistry, enabling direct access to substituted indole scaffolds through standard functional group transformations. Its ortho-dimethoxy substitution pattern enhances solubility and stability while maintaining reactivity in electrophilic aromatic substitution and transition-metal-catalyzed coupling reactions. The molecule functions as a versatile intermediate for the synthesis of heterocyclic compounds and bioactive molecules, offering predictable regioselectivity and ease of purification under routine bench conditions.
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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: