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Structure of 1934432-59-3
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tert-Butyl 7-amino-1H-indole-1-carboxylate features a bench-stable indole core with a strategically positioned amino group at the C7 position, enabling direct functionalization in late-stage diversification. The tert-butyl ester serves as a robust protecting group for the carboxylic acid, readily cleaved under mild acidic conditions without affecting sensitive heterocyclic moieties. This derivative supports efficient access to complex indole-based architectures in medicinal chemistry and materials synthesis.
tert-Butyl 7-amino-1H-indole-1-carboxylate serves as a versatile building block for indole-based scaffolds, enabling direct functionalization at the 7-position. The tert-butyl carbamate group provides excellent stability and ease of removal under mild acidic conditions, while the primary amine facilitates coupling reactions and derivatization. This compound is well-suited for medicinal chemistry campaigns requiring access to substituted indoles via standard reductive amination, Buchwald-Hartwig, or electrophilic substitution protocols.
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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: