(S)-2-(Tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid
95%
- Product Code: 52890
CAS:
790305-00-9
| Molecular Weight: | 273.3 g./mol | Molecular Formula: | C₁₃H₂₃NO₅ |
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| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the preparation of peptide-based compounds. It serves as a key intermediate in the construction of complex molecules, enabling the introduction of specific functional groups that are essential for biological activity. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a pent-4-enyloxy moiety, makes it valuable for selective deprotection and further functionalization during synthetic processes. Additionally, it is employed in the development of pharmaceuticals, where it contributes to the synthesis of active pharmaceutical ingredients (APIs) with potential therapeutic applications. Its compatibility with various reaction conditions and its role in facilitating controlled chemical transformations make it a versatile tool in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿43,200.00 |
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(S)-2-(Tert-butoxycarbonylamino)-3-(pent-4-enyloxy)propanoic acid
This chemical is primarily utilized in the field of organic synthesis, particularly in the preparation of peptide-based compounds. It serves as a key intermediate in the construction of complex molecules, enabling the introduction of specific functional groups that are essential for biological activity. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a pent-4-enyloxy moiety, makes it valuable for selective deprotection and further functionalization during synthetic processes. Additionally, it is employed in the development of pharmaceuticals, where it contributes to the synthesis of active pharmaceutical ingredients (APIs) with potential therapeutic applications. Its compatibility with various reaction conditions and its role in facilitating controlled chemical transformations make it a versatile tool in medicinal chemistry and drug discovery.
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