tert-Butyl 4-(2-((tert-butoxycarbonyl)amino)-3-methoxy-3-oxopropyl)-1H-imidazole-1-carboxylate
95%
- Product Code: 104579
CAS:
165062-56-6
| Molecular Weight: | 369.41 g./mol | Molecular Formula: | C₁₇H₂₇N₃O₆ |
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| EC Number: | MDL Number: | MFCD02668181 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.17±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis as a protected intermediate for the preparation of more complex molecules. It is particularly valuable in peptide and heterocycle chemistry, where the tert-butyl and tert-butoxycarbonyl (Boc) groups serve as protective groups for amines and carboxylic acids, respectively. These protecting groups are crucial in multi-step synthetic processes, as they prevent unwanted reactions at specific sites while allowing modifications at other positions. The compound is often employed in the synthesis of biologically active compounds, including pharmaceuticals and agrochemicals, where precise control over functional group reactivity is essential. Additionally, its imidazole moiety makes it a potential building block for the development of compounds with pharmacological or catalytic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $77.23 |
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| 0.250 | 10-20 days | $140.41 |
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| 1.000 | 10-20 days | $280.83 |
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tert-Butyl 4-(2-((tert-butoxycarbonyl)amino)-3-methoxy-3-oxopropyl)-1H-imidazole-1-carboxylate
This chemical is primarily used in organic synthesis as a protected intermediate for the preparation of more complex molecules. It is particularly valuable in peptide and heterocycle chemistry, where the tert-butyl and tert-butoxycarbonyl (Boc) groups serve as protective groups for amines and carboxylic acids, respectively. These protecting groups are crucial in multi-step synthetic processes, as they prevent unwanted reactions at specific sites while allowing modifications at other positions. The compound is often employed in the synthesis of biologically active compounds, including pharmaceuticals and agrochemicals, where precise control over functional group reactivity is essential. Additionally, its imidazole moiety makes it a potential building block for the development of compounds with pharmacological or catalytic properties.
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