Methyl 2-(aminomethyl)-1H-imidazole-4-carboxylate, 2-BOC protected

95%

Reagent Code: #42850
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CAS Number 252348-76-8

science Other reagents with same CAS 252348-76-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.27 g/mol
Formula C₁₁H₁₇N₃O₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules, particularly in pharmaceutical research. Its BOC-protected amine group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes. It is often employed in the development of imidazole-based compounds, which are known for their biological activity, including applications in drug discovery for targeting enzymes and receptors. The carboxylate group further enhances its versatility, allowing for modifications and conjugation with other chemical entities. Its role is crucial in the synthesis of potential therapeutic agents, particularly in the fields of oncology, neurology, and infectious diseases.

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inventory 250mg
10-20 days ฿31,077.00

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Methyl 2-(aminomethyl)-1H-imidazole-4-carboxylate, 2-BOC protected
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This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules, particularly in pharmaceutical research. Its BOC-protected amine group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes. It is often employed in the development of imidazole-based compounds, which are known for their biological activity, including applications in drug discovery for targeting enzymes and receptors. The carboxylate gr

This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules, particularly in pharmaceutical research. Its BOC-protected amine group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes. It is often employed in the development of imidazole-based compounds, which are known for their biological activity, including applications in drug discovery for targeting enzymes and receptors. The carboxylate group further enhances its versatility, allowing for modifications and conjugation with other chemical entities. Its role is crucial in the synthesis of potential therapeutic agents, particularly in the fields of oncology, neurology, and infectious diseases.

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