(2S,5R)-Benzhydryl 3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4-oxide
≥95%
- Product Code: 70882
CAS:
87579-78-0
| Molecular Weight: | 383.46 g./mol | Molecular Formula: | C₂₁H₂₁NO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11044527 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the synthesis of beta-lactam antibiotics, which are crucial for treating bacterial infections. Its structure serves as a key intermediate in the production of penicillins and cephalosporins, enabling the development of broad-spectrum antibiotics. The compound's unique bicyclic structure and functional groups make it valuable for modifying antibiotic properties, such as enhancing stability against beta-lactamases and improving efficacy against resistant bacterial strains. Additionally, it is employed in pharmaceutical research to explore new derivatives with improved pharmacokinetic profiles and reduced side effects. Its role in antibiotic development underscores its importance in addressing global health challenges related to bacterial resistance.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿531.00 |
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| 1.000 | 10-20 days | ฿1,062.00 |
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| 5.000 | 10-20 days | ฿3,258.00 |
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(2S,5R)-Benzhydryl 3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4-oxide
This compound is primarily utilized in the synthesis of beta-lactam antibiotics, which are crucial for treating bacterial infections. Its structure serves as a key intermediate in the production of penicillins and cephalosporins, enabling the development of broad-spectrum antibiotics. The compound's unique bicyclic structure and functional groups make it valuable for modifying antibiotic properties, such as enhancing stability against beta-lactamases and improving efficacy against resistant bacterial strains. Additionally, it is employed in pharmaceutical research to explore new derivatives with improved pharmacokinetic profiles and reduced side effects. Its role in antibiotic development underscores its importance in addressing global health challenges related to bacterial resistance.
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