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Catalog Number:
41626
CAS Number:
36923-21-4
7β-amino-3-céphème-4-carboxylate de diphénylméthyle
Purity:
≥ 98 % (HPLC)
Synonym(s):
Benzhydryl(6 R ,7 R )-7-Amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ène-2-carboxylate, Ester benzhydrylique de l'acide (6 R ,7 R )-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ène-2-carboxylique, Ester diphénylméthylique de l'acide 7β-amino-3-céphème-4-carboxylique
Documents
$145.52 /1G
Taille
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Informations sur le produit

Diphenylmethyl 7b-amino-3-cephem-4-carboxylate is a versatile compound recognized for its significant role in the development of cephalosporin antibiotics. This compound features a unique structure that enhances its antibacterial properties, making it a valuable asset in pharmaceutical research and development. Its ability to inhibit bacterial cell wall synthesis positions it as a crucial ingredient in formulations aimed at combating a wide range of bacterial infections.

Researchers and industry professionals can leverage Diphenylmethyl 7b-amino-3-cephem-4-carboxylate in the synthesis of novel cephalosporin derivatives, potentially leading to the creation of more effective antibiotics with improved efficacy and reduced resistance. Its stability and compatibility with various chemical processes make it an ideal candidate for further exploration in medicinal chemistry. The compound's unique properties not only facilitate the development of new therapeutic agents but also enhance existing formulations, providing a competitive edge in the pharmaceutical market.

Numéro CAS 
36923-21-4
Formule moléculaire
C20H18N2O3S
Poids moléculaire 
366.44
Point de fusion 
164 - 168 °C
Rotation optique 
[a]20D = 50 - 55 ° (C = 1 dans CHCL3)
Informations générales
Numéro CAS 
36923-21-4
Formule moléculaire
C20H18N2O3S
Poids moléculaire 
366.44
Point de fusion 
164 - 168 °C
Rotation optique 
[a]20D = 50 - 55 ° (C = 1 dans CHCL3)
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

Diphenylmethyl 7b-amino-3-cephem-4-carboxylate is widely utilized in research focused on:

  • Antibiotic Development: This compound serves as a precursor in the synthesis of novel cephalosporin antibiotics, which are crucial for treating bacterial infections. Its structure allows for modifications that enhance antibacterial activity.
  • Pharmaceutical Formulations: It is used in the formulation of various pharmaceutical products, providing stability and improved bioavailability compared to other compounds in the same class.
  • Research in Medicinal Chemistry: Researchers leverage its unique chemical properties to explore new therapeutic agents, particularly in combating antibiotic resistance, a growing concern in healthcare.
  • Biochemical Studies: The compound is valuable in biochemical research for studying enzyme interactions and mechanisms, aiding in the understanding of drug action at the molecular level.
  • Industrial Applications: Beyond pharmaceuticals, it finds applications in the development of agrochemicals, where its properties can be tailored for pest control solutions, offering an environmentally friendly alternative.

Citations