(R)-4-Nitrobenzyl 2-diazo-4-((2R,3S)-3-((R)-1-hydroxy-ethyl)-4-oxoazetidin-2-yl)-3-oxopentanoate
98%
- Product Code: 37687
CAS:
137391-68-5
| Molecular Weight: | 390.36 g./mol | Molecular Formula: | C₁₇H₁₈N₄O₇ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11111990 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of beta-lactam antibiotics, which are crucial for treating bacterial infections. Its structure, featuring a diazo group and a beta-lactam ring, makes it a valuable intermediate in the development of novel antibiotic agents. The compound is often employed in organic synthesis to introduce the beta-lactam moiety into more complex molecules, enhancing their biological activity. Additionally, its chiral centers allow for the production of enantiomerically pure antibiotics, which can improve efficacy and reduce side effects. It is also explored in research for developing enzyme inhibitors and studying mechanisms of antibiotic resistance.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $222.98 |
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(R)-4-Nitrobenzyl 2-diazo-4-((2R,3S)-3-((R)-1-hydroxy-ethyl)-4-oxoazetidin-2-yl)-3-oxopentanoate
This compound is primarily utilized in the synthesis of beta-lactam antibiotics, which are crucial for treating bacterial infections. Its structure, featuring a diazo group and a beta-lactam ring, makes it a valuable intermediate in the development of novel antibiotic agents. The compound is often employed in organic synthesis to introduce the beta-lactam moiety into more complex molecules, enhancing their biological activity. Additionally, its chiral centers allow for the production of enantiomerically pure antibiotics, which can improve efficacy and reduce side effects. It is also explored in research for developing enzyme inhibitors and studying mechanisms of antibiotic resistance.
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