tert-Butyl ((R)-1-((S)-oxiran-2-yl)-2-phenylethyl)carbamate
97%
- Product Code: 70758
CAS:
156474-22-5
| Molecular Weight: | 263.33 g./mol | Molecular Formula: | C₁₅H₂₁NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08061626 | |
| Melting Point: | Boiling Point: | 398.8±25.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of chiral intermediates. Its structure, featuring both an oxirane ring and a carbamate group, makes it a valuable building block in asymmetric synthesis. It is often employed in the production of biologically active molecules, such as β-amino alcohols, which are key components in drugs targeting cardiovascular diseases, central nervous system disorders, and infections. Additionally, its stereochemical properties enable its use in the preparation of enantiomerically pure compounds, enhancing the efficacy and specificity of therapeutic agents. The compound is also explored in medicinal chemistry research for designing novel inhibitors and enzyme modulators.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,500.00 |
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| 0.250 | 10-20 days | ฿11,200.00 |
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tert-Butyl ((R)-1-((S)-oxiran-2-yl)-2-phenylethyl)carbamate
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of chiral intermediates. Its structure, featuring both an oxirane ring and a carbamate group, makes it a valuable building block in asymmetric synthesis. It is often employed in the production of biologically active molecules, such as β-amino alcohols, which are key components in drugs targeting cardiovascular diseases, central nervous system disorders, and infections. Additionally, its stereochemical properties enable its use in the preparation of enantiomerically pure compounds, enhancing the efficacy and specificity of therapeutic agents. The compound is also explored in medicinal chemistry research for designing novel inhibitors and enzyme modulators.
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