Methyl 4-((tert-butoxycarbonyl)amino)-1-methyl-1H-imidazole-2-carboxylate
98%
- Product Code: 46050
CAS:
500701-36-0
| Molecular Weight: | 255.2704 g./mol | Molecular Formula: | C₁₁H₁₇N₃O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08275080 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in organic synthesis as an intermediate in the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a key building block for the development of biologically active compounds, including potential drug candidates. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and an imidazole ring, makes it valuable in peptide and heterocycle chemistry. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. This chemical is often employed in the synthesis of imidazole-based derivatives, which are known for their diverse pharmacological properties, such as anti-inflammatory, antiviral, and anticancer activities. Additionally, its stability and reactivity make it a useful reagent in medicinal chemistry for exploring structure-activity relationships and optimizing drug-like properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,453.00 |
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Methyl 4-((tert-butoxycarbonyl)amino)-1-methyl-1H-imidazole-2-carboxylate
This compound is primarily used in organic synthesis as an intermediate in the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a key building block for the development of biologically active compounds, including potential drug candidates. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and an imidazole ring, makes it valuable in peptide and heterocycle chemistry. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. This chemical is often employed in the synthesis of imidazole-based derivatives, which are known for their diverse pharmacological properties, such as anti-inflammatory, antiviral, and anticancer activities. Additionally, its stability and reactivity make it a useful reagent in medicinal chemistry for exploring structure-activity relationships and optimizing drug-like properties.
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