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Catalog Number:
44490
CAS Number:
104146-10-3
4-méthoxybenzyle 3-chlorométhyl-7-(2-phénylacétamido)-3-céphème-4-carboxylate
Purity:
≥ 98%
Synonym(s):
Ester 4-méthoxybenzylique de l'acide 3-chlorométhyl-7-(2-phénylacétamido)-3-céphème-4-carboxylique
Documents
$46.07 /5G
Taille
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Informations sur le produit

4-Methoxybenzyl 3-Chloromethyl-7-(2-phenylacetamido)-3-cephem-4-carboxylate is a versatile compound with significant applications in pharmaceutical research and development. This compound, known for its unique structure, features a methoxy group that enhances its solubility and bioavailability, making it an attractive candidate for antibiotic formulations. Its chloromethyl and phenylacetamido substituents contribute to its efficacy in targeting bacterial infections, particularly in the development of cephalosporin antibiotics. Researchers have utilized this compound in the synthesis of novel antibacterial agents, demonstrating its potential to combat resistant strains of bacteria.

In addition to its pharmaceutical applications, this compound can be explored in the field of medicinal chemistry for the design of new therapeutic agents. Its structural characteristics allow for modifications that can lead to improved pharmacological profiles. The ability to fine-tune its properties makes it a valuable tool for researchers aiming to develop more effective treatments. With its promising applications in drug discovery and development, 4-Methoxybenzyl 3-Chloromethyl-7-(2-phenylacetamido)-3-cephem-4-carboxylate stands out as a compound of interest for professionals in the pharmaceutical industry.

Numéro CAS 
104146-10-3
Formule moléculaire
C24H23ClN2O5S
Poids moléculaire 
486.97
Point de fusion 
153 °C (déc.)
Informations générales
Numéro CAS 
104146-10-3
Formule moléculaire
C24H23ClN2O5S
Poids moléculaire 
486.97
Point de fusion 
153 °C (déc.)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

4-Methoxybenzyl 3-Chloromethyl-7-(2-phenylacetamido)-3-cephem-4-carboxylate is widely utilized in research focused on:

  • Antibiotic Development: This compound serves as a key intermediate in synthesizing cephalosporin antibiotics, which are crucial for treating bacterial infections.
  • Pharmaceutical Formulations: It is used in the formulation of drugs, enhancing the efficacy and stability of active ingredients in various therapeutic applications.
  • Biochemical Research: Researchers employ this compound to study enzyme interactions and mechanisms, contributing to advancements in drug discovery and development.
  • Analytical Chemistry: It acts as a standard in analytical methods, aiding in the quality control of pharmaceutical products and ensuring compliance with regulatory standards.
  • Medicinal Chemistry: The compound is explored for its potential in developing new antimicrobial agents, addressing the growing concern of antibiotic resistance.

Citations