N-Boc-D-2-amino-2-cyclohexylethanol
≥95%,≥99%e.e.
- Product Code: 71228
CAS:
188348-00-7
| Molecular Weight: | 243.3 g./mol | Molecular Formula: | C₁₃H₂₅NO₃ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 83-87°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
N-Boc-D-2-amino-2-cyclohexylethanol is primarily used as a chiral building block in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as an intermediate in the production of enantiomerically pure compounds, which are crucial for developing drugs with specific biological activities. The Boc (tert-butoxycarbonyl) protecting group ensures selective reactions during synthesis, allowing for the precise construction of target molecules. This compound is often employed in the preparation of peptidomimetics, bioactive peptides, and other therapeutic agents where the stereochemistry of the molecule plays a critical role in its efficacy. Its cyclohexyl group contributes to the lipophilicity of the resulting compounds, influencing their pharmacokinetic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €125.37 |
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| 5.000 | 10-20 days | €352.83 |
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N-Boc-D-2-amino-2-cyclohexylethanol
N-Boc-D-2-amino-2-cyclohexylethanol is primarily used as a chiral building block in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as an intermediate in the production of enantiomerically pure compounds, which are crucial for developing drugs with specific biological activities. The Boc (tert-butoxycarbonyl) protecting group ensures selective reactions during synthesis, allowing for the precise construction of target molecules. This compound is often employed in the preparation of peptidomimetics, bioactive peptides, and other therapeutic agents where the stereochemistry of the molecule plays a critical role in its efficacy. Its cyclohexyl group contributes to the lipophilicity of the resulting compounds, influencing their pharmacokinetic properties.
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