3-((tert-Butoxycarbonyl)amino)-3-(furan-2-yl)propanoic acid
97%
- Product Code: 44167
CAS:
14676-03-0
| Molecular Weight: | 255.27 g./mol | Molecular Formula: | C₁₂H₁₇NO₅ |
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| EC Number: | MDL Number: | MFCD02090673 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a furan moiety, makes it valuable in peptide synthesis and medicinal chemistry. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the furan ring provides a versatile handle for further chemical modifications, such as cyclization or coupling reactions, making it useful in the development of pharmaceuticals, agrochemicals, and other biologically active compounds. Its application is particularly relevant in the synthesis of heterocyclic compounds and peptidomimetics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿16,596.00 |
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| 0.250 | 10-20 days | ฿24,894.00 |
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| 1.000 | 10-20 days | ฿62,235.00 |
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3-((tert-Butoxycarbonyl)amino)-3-(furan-2-yl)propanoic acid
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a furan moiety, makes it valuable in peptide synthesis and medicinal chemistry. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the furan ring provides a versatile handle for further chemical modifications, such as cyclization or coupling reactions, making it useful in the development of pharmaceuticals, agrochemicals, and other biologically active compounds. Its application is particularly relevant in the synthesis of heterocyclic compounds and peptidomimetics.
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