N-Boc-(S)-2-amino-3-benzyloxy-1-propanol
97%
- Product Code: 50159
CAS:
79069-15-1
| Molecular Weight: | 281.35 g./mol | Molecular Formula: | C₁₅H₂₃NO₄ |
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| EC Number: | MDL Number: | MFCD00235945 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.105g/cm3 | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
N-Boc-(S)-2-amino-3-benzyloxy-1-propanol is widely used in organic synthesis, particularly in the preparation of chiral compounds. It serves as a key intermediate in the synthesis of pharmaceuticals, especially in the development of drugs that require enantiomerically pure substances. The compound is often employed in peptide synthesis, where it acts as a protected amino alcohol, facilitating the construction of complex peptide chains. Additionally, it is utilized in the production of bioactive molecules and natural products, where its stereochemistry and functional groups play a crucial role in achieving the desired biological activity. The benzyloxy group provides a protective function, which can be selectively removed under specific conditions, allowing for further chemical modifications. This makes it a versatile building block in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,376.00 |
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| 5.000 | 10-20 days | ฿7,308.00 |
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| 10.000 | 10-20 days | ฿14,400.00 |
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N-Boc-(S)-2-amino-3-benzyloxy-1-propanol
N-Boc-(S)-2-amino-3-benzyloxy-1-propanol is widely used in organic synthesis, particularly in the preparation of chiral compounds. It serves as a key intermediate in the synthesis of pharmaceuticals, especially in the development of drugs that require enantiomerically pure substances. The compound is often employed in peptide synthesis, where it acts as a protected amino alcohol, facilitating the construction of complex peptide chains. Additionally, it is utilized in the production of bioactive molecules and natural products, where its stereochemistry and functional groups play a crucial role in achieving the desired biological activity. The benzyloxy group provides a protective function, which can be selectively removed under specific conditions, allowing for further chemical modifications. This makes it a versatile building block in medicinal chemistry and drug discovery processes.
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