(3R,4S)-tert-Butyl 2-oxo-4-phenyl-3-(triethylsilyloxy)azetidine-1-carboxylate
99%
- Product Code: 36753
CAS:
149198-47-0
| Molecular Weight: | 377.55 g./mol | Molecular Formula: | C₂₀H₃₁NO₄Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08273948 | |
| Melting Point: | Boiling Point: | 463ºC at 760 mmHg | |
| Density: | Storage Condition: | -20 ℃ |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of β-lactam antibiotics, which are essential for treating bacterial infections. The tert-butyl and triethylsilyl groups provide steric protection, enhancing the stability and selectivity of the compound during chemical reactions. Its structural features make it valuable in asymmetric synthesis, enabling the creation of chiral molecules with high enantiomeric purity. Additionally, it is employed in research and development for designing novel drug candidates, particularly those targeting bacterial resistance mechanisms. Its role in facilitating efficient and controlled reactions underscores its importance in advanced organic chemistry applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless - Slightly pale yellow Clear Liquid |
| PURITY | 99-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $49.83 |
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| 1.000 | 10-20 days | $80.98 |
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| 5.000 | 10-20 days | $287.38 |
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(3R,4S)-tert-Butyl 2-oxo-4-phenyl-3-(triethylsilyloxy)azetidine-1-carboxylate
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of β-lactam antibiotics, which are essential for treating bacterial infections. The tert-butyl and triethylsilyl groups provide steric protection, enhancing the stability and selectivity of the compound during chemical reactions. Its structural features make it valuable in asymmetric synthesis, enabling the creation of chiral molecules with high enantiomeric purity. Additionally, it is employed in research and development for designing novel drug candidates, particularly those targeting bacterial resistance mechanisms. Its role in facilitating efficient and controlled reactions underscores its importance in advanced organic chemistry applications.
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