(R)-2-((Tert-Butoxycarbonyl)Amino)-2-Methylpent-4-Enoic Acid
≥97%
- Product Code: 104216
CAS:
129786-68-1
| Molecular Weight: | 229.27 g./mol | Molecular Formula: | C₁₁H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02682443 | |
| Melting Point: | Boiling Point: | 359.1±35.0 °C(Predicted) | |
| Density: | 1.080±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a reactive double bond, makes it a valuable intermediate in peptide synthesis and the construction of complex organic frameworks. The Boc group ensures selective deprotection during synthetic processes, while the pentenoic acid moiety allows for further functionalization, such as through olefin metathesis or Michael addition reactions. This chemical is often employed in the synthesis of chiral compounds, where its stereocenter plays a critical role in achieving enantioselectivity. Additionally, it is used in the preparation of inhibitors, receptor ligands, and other biologically active molecules, contributing to advancements in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,340.00 |
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(R)-2-((Tert-Butoxycarbonyl)Amino)-2-Methylpent-4-Enoic Acid
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a reactive double bond, makes it a valuable intermediate in peptide synthesis and the construction of complex organic frameworks. The Boc group ensures selective deprotection during synthetic processes, while the pentenoic acid moiety allows for further functionalization, such as through olefin metathesis or Michael addition reactions. This chemical is often employed in the synthesis of chiral compounds, where its stereocenter plays a critical role in achieving enantioselectivity. Additionally, it is used in the preparation of inhibitors, receptor ligands, and other biologically active molecules, contributing to advancements in medicinal chemistry and drug discovery.
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