4-cyanomethyl-imidazole-1-carboxylic acid tert-butyl ester

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Reagent Code: #157333
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CAS Number 367267-46-7

science Other reagents with same CAS 367267-46-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.232 g/mol
Formula C₁₀H₁₃N₃O₂
inventory_2 Storage & Handling
Storage 2-8°C

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 imidazole core allows for hydrogen bonding and coordination with metal ions, making it valuable in drug design. The tert-butyl ester group acts as a protecting group, enabling selective reactions in multi-step syntheses. The nitrile (cyano) functionality can be further modified to introduce amides, amines, or heterocyclic structures, enhancing molecular diversity in medicinal chemistry research. Commonly employed in the preparation of protease inhibitors and anti-inflammatory agents.

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inventory 100mg
10-20 days ฿20,000.00

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4-cyanomethyl-imidazole-1-carboxylic acid tert-butyl ester
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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 imidazole core allows for hydrogen bonding and coordination with metal ions, making it valuable in drug design. The tert-butyl ester group acts as a protecting group, enabling selective reactions in multi-step syntheses. The nitrile (cyano) functionality can be further modified to introduce amides, amines, or heterocyclic structures, enhan

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its imidazole core allows for hydrogen bonding and coordination with metal ions, making it valuable in drug design. The tert-butyl ester group acts as a protecting group, enabling selective reactions in multi-step syntheses. The nitrile (cyano) functionality can be further modified to introduce amides, amines, or heterocyclic structures, enhancing molecular diversity in medicinal chemistry research. Commonly employed in the preparation of protease inhibitors and anti-inflammatory agents.

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