(5R,6S)-3-((2-Formimidamidoethyl)thio)-6-((R)-1-hydroxyethyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid hydrate
98%
- Product Code: 51693
Alias:
Related CAS number: 64221-86-9
CAS:
74431-23-5
Molecular Weight: | 317.36 g./mol | Molecular Formula: | C₁₂H₁₉N₃O₅S |
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EC Number: | MDL Number: | ||
Melting Point: | 193-198°C | Boiling Point: | 567.3°C |
Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of beta-lactam antibiotics. Its structure is crucial for developing antibiotics that target a wide range of bacterial infections, particularly those resistant to other treatments. The compound's unique bicyclic structure enhances its ability to inhibit bacterial cell wall synthesis, making it effective against both Gram-positive and Gram-negative bacteria. It is often employed in research and development to create new formulations of antibiotics, aiming to improve efficacy and reduce resistance. Additionally, it plays a role in the production of carbapenems, a class of antibiotics known for their broad-spectrum activity and stability against beta-lactamases.
Product Specification:
Test | Specification |
---|---|
Purity | 98-100 |
MELTING POINT | 193-198 |
APPEARANCE | SOLID |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.025 | 10-20 days | ฿1,280.00 |
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0.050 | 10-20 days | ฿2,260.00 |
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0.250 | 10-20 days | ฿6,780.00 |
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1.000 | 10-20 days | ฿14,290.00 |
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(5R,6S)-3-((2-Formimidamidoethyl)thio)-6-((R)-1-hydroxyethyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid hydrate
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of beta-lactam antibiotics. Its structure is crucial for developing antibiotics that target a wide range of bacterial infections, particularly those resistant to other treatments. The compound's unique bicyclic structure enhances its ability to inhibit bacterial cell wall synthesis, making it effective against both Gram-positive and Gram-negative bacteria. It is often employed in research and development to create new formulations of antibiotics, aiming to improve efficacy and reduce resistance. Additionally, it plays a role in the production of carbapenems, a class of antibiotics known for their broad-spectrum activity and stability against beta-lactamases.
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