tert-Butyl 2-((tert-butoxycarbonyl)amino)-1H-imidazole-1-carboxylate

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Reagent Code: #41171
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CAS Number 1186299-71-7

science Other reagents with same CAS 1186299-71-7

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Weight 283.3235 g/mol
Formula C₁₃H₂₁N₃O₄
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description Product Description

This compound is a doubly protected derivative of 2-amino-1H-imidazole, with tert-butoxycarbonyl (Boc) groups on both the 2-amino functionality and the N1 position. It is primarily utilized in organic synthesis as a building block, particularly in peptide chemistry, where it safeguards the amino and imidazole nitrogen groups during complex reactions, enabling selective transformations without unwanted side reactions. Its stability under various conditions makes it suitable for multi-step synthesis processes. Additionally, it is employed in the preparation of heterocyclic compounds, where the protecting groups are essential for achieving high yields and purity. Its application is also prominent in medicinal chemistry for developing pharmaceutical intermediates.

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inventory 100mg
10-20 days ฿2,952.00

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tert-Butyl 2-((tert-butoxycarbonyl)amino)-1H-imidazole-1-carboxylate
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This compound is a doubly protected derivative of 2-amino-1H-imidazole, with tert-butoxycarbonyl (Boc) groups on both the 2-amino functionality and the N1 position. It is primarily utilized in organic synthesis as a building block, particularly in peptide chemistry, where it safeguards the amino and imidazole nitrogen groups during complex reactions, enabling selective transformations without unwanted side reactions. Its stability under various conditions makes it suitable for multi-step synthesis proces

This compound is a doubly protected derivative of 2-amino-1H-imidazole, with tert-butoxycarbonyl (Boc) groups on both the 2-amino functionality and the N1 position. It is primarily utilized in organic synthesis as a building block, particularly in peptide chemistry, where it safeguards the amino and imidazole nitrogen groups during complex reactions, enabling selective transformations without unwanted side reactions. Its stability under various conditions makes it suitable for multi-step synthesis processes. Additionally, it is employed in the preparation of heterocyclic compounds, where the protecting groups are essential for achieving high yields and purity. Its application is also prominent in medicinal chemistry for developing pharmaceutical intermediates.

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