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Structure of 1481631-51-9
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tert-Butyl 4-formyl-5-methoxy-7-methyl-1H-indole-1-carboxylate features a formyl group at C4, a methoxy substituent at C5, and a methyl group at C7 on the indole core, enabling direct functionalization in late-stage diversification. The tert-butyl ester provides stability and ease of deprotection under mild acidic conditions. This scaffold supports rapid access to biologically active indole derivatives.
tert-Butyl 4-formyl-5-methoxy-7-methyl-1H-indole-1-carboxylate serves as a versatile building block for indole-based scaffolds, enabling efficient access to functionalized heterocycles via formyl group reactivity. The protected indole core exhibits bench stability and tolerates diverse reaction conditions, facilitating subsequent transformations such as reductive amination, Mannich reactions, or coupling protocols. Its methoxy and methyl substituents provide defined electronic and steric profiles, enhancing synthetic predictability in medicinal chemistry and process development workflows.
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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: