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Structure of 49761-82-2
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tert-Butyl 1H-imidazole-1-carboxylate serves as a stable, bench-ready imidazole protecting group for amine-directed functionalization. The tert-butyl ester moiety enables orthogonal deprotection under mild acidic conditions, preserving sensitive functionalities. This derivative integrates seamlessly into synthetic sequences requiring selective imidazole incorporation, particularly in medicinal chemistry and peptide modification workflows.
tert-Butyl 1H-imidazole-1-carboxylate serves as a stable, bench-ready imidazole protecting group derivative, enabling selective functionalization at the nitrogen atom. It facilitates efficient N-alkylation and transition-metal-catalyzed coupling reactions while maintaining compatibility with diverse reaction conditions. The tert-butyl ester moiety allows for straightforward deprotection under mild acidic conditions, making it ideal for constructing imidazole-containing scaffolds in medicinal chemistry and catalyst design.
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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: