100680-33-9 | 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-(2-furanyl)-2-(methoxyimino)acetyl]amino]-8-oxo-, 1-(2-methoxy-2-methyl-1-oxopropoxy)ethyl ester, (6R,7R)-

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Description

• Catalog Number: BE00394
• Chemical Name: 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-(2-furanyl)-2-(methoxyimino)acetyl]amino]-8-oxo-, 1-(2-methoxy-2-methyl-1-oxopropoxy)ethyl ester, (6R,7R)-
• CAS Number: 100680-33-9
• Molecular Formula: C23H28N4O11S
• Molecular Weight: 568.5536
• SMILES: CO/N=C(\C(=O)N[C@@H]1C(=O)N2[C@@H]1SCC(=C2C(=O)OC(OC(=O)C(OC)(C)C)C)COC(=O)N)/c1ccco1

Upstream Synthesis Route

Cefuroxime pivoxetil, a prodrug of the antibiotic cefuroxime, plays a crucial role in chemical synthesis as a versatile intermediate. It is commonly utilized for the preparation of various cefuroxime derivatives by selective chemical modifications. The pivoxetil moiety in its structure allows for easy manipulation and incorporation of different functional groups, making it highly adaptable for creating new compounds with enhanced pharmacological properties. In synthetic chemistry, cefuroxime pivoxetil serves as a valuable building block for the development of novel antibacterial agents and other bioactive molecules through strategic structural alterations and derivatization strategies. Its unique chemical reactivity and compatibility with diverse synthetic methodologies make it a valuable tool in the synthesis of complex organic molecules with potential therapeutic applications. By exploiting its synthetic utility, researchers can explore the synthesis of structurally diverse compounds for addressing emerging challenges in drug discovery and medicinal chemistry.