The product is High Quality (3r,4s)-1-benzoyl-4-phenyl-3-[(triethylsilyl)oxy]-2-azetidinone with the CAS number 149249-91-2. It is offered at the best price in the market. This azetidinone derivative is known for its high purity and quality, which ensures reliable performance in various applications.
The molecular formula of (3r,4s)-1-benzoyl-4-phenyl-3-[(triethylsilyl)oxy]-2-azetidinone can be determined based on its chemical structure. The compound has a specific molecular weight that is important for accurate dosing and reaction stoichiometry in chemical processes. The product is typically supplied in a form that is stable under normal storage conditions and has a defined shelf - life.
This azetidinone compound has a wide range of uses in the field of organic synthesis. It can serve as a key intermediate in the synthesis of various pharmaceuticals. For example, it can be used in the preparation of antibiotics, where the azetidinone ring structure is a crucial part of the active pharmaceutical ingredient. The presence of the benzoyl and phenyl groups, as well as the triethylsilyl - protected hydroxyl group, provides unique reactivity and selectivity in chemical reactions.
In addition to pharmaceuticals, it can also be used in the development of new materials. The compound's chemical properties make it suitable for use in the synthesis of specialty polymers or functional materials with specific properties such as enhanced solubility or reactivity.
When using (3r,4s)-1-benzoyl-4-phenyl-3-[(triethylsilyl)oxy]-2-azetidinone, it is important to follow proper laboratory safety procedures. Wear appropriate personal protective equipment, including gloves, safety glasses, and a lab coat. The product should be stored in a cool, dry place away from sources of heat and ignition.
In chemical reactions, the compound should be added to the reaction mixture slowly and carefully, taking into account the reaction conditions such as temperature, solvent, and catalysts. The amount of the product used should be accurately measured based on the reaction requirements. After the reaction, the product can be purified using standard purification techniques such as column chromatography or recrystallization.
Case Study 1: Pharmaceutical Synthesis
In a pharmaceutical research project, (3r,4s)-1-benzoyl-4-phenyl-3-[(triethylsilyl)oxy]-2-azetidinone was used as an intermediate in the synthesis of a new antibiotic. The researchers first deprotected the triethylsilyl group under specific reaction conditions to expose the hydroxyl group. Then, they carried out a series of reactions to couple the azetidinone with other chemical moieties to form the final antibiotic compound. The high purity of the starting azetidinone product ensured a high yield and purity of the final antibiotic, which showed promising antibacterial activity in in - vitro tests.
Case Study 2: Material Development
A research team was working on the development of a new type of polymer with enhanced solubility in organic solvents. They used (3r,4s)-1-benzoyl-4-phenyl-3-[(triethylsilyl)oxy]-2-azetidinone as a monomer in the polymerization reaction. By carefully controlling the reaction conditions, they were able to incorporate the azetidinone unit into the polymer backbone. The resulting polymer had improved solubility and showed potential applications in coatings and adhesives.
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