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Structure of 184031-16-1
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tert-Butyl 1H-indol-5-ylcarbamate features a protected indole nitrogen and a tert-butyl carbamate group, enabling stable incorporation into complex molecular architectures. This derivative serves as a key intermediate in the synthesis of functionalized indoles, particularly in medicinal chemistry applications where selective N-acylation or cross-coupling reactions are required under standard conditions.
tert-Butyl 1H-indol-5-ylcarbamate serves as a stable, bench-ready building block for indole-based medicinal chemistry. The tert-butyl carbamate group provides orthogonal protection for primary amines, enabling selective functionalization at the indole C5 position. It facilitates Pd-catalyzed cross-coupling reactions and supports downstream transformations such as deprotection to the free amine or incorporation into heterocyclic scaffolds. Its stability under standard reaction conditions and ease of purification make it ideal for multi-step synthesis workflows in API development.
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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: