Ethyl 4-((tert-butoxycarbonyl)amino)-1-methyl-1H-imidazole-2-carboxylate

98%

Reagent Code: #184642
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CAS Number 128293-63-0

science Other reagents with same CAS 128293-63-0

blur_circular Chemical Specifications

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Weight 269.30 g/mol
Formula C₁₂H₁₉N₃O₄
badge Registry Numbers
MDL Number MFCD16876078
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its protected amine and ester functionalities allow for selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing imidazole-based scaffolds, which are prevalent in drugs targeting inflammation, cancer, and infectious diseases. The Boc-protected amine ensures stability during reactions and can be deprotected under mild acidic conditions to enable further derivatization.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,850.00
inventory 25g
10-20 days ฿28,340.00

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Ethyl 4-((tert-butoxycarbonyl)amino)-1-methyl-1H-imidazole-2-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its protected amine and ester functionalities allow for selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing imidazole-based scaffolds, which are prevalent in drugs targeting inflammation, cancer, and infectious diseases. The Boc-protected amine ensures stability during reactions and ca

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its protected amine and ester functionalities allow for selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing imidazole-based scaffolds, which are prevalent in drugs targeting inflammation, cancer, and infectious diseases. The Boc-protected amine ensures stability during reactions and can be deprotected under mild acidic conditions to enable further derivatization.

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