88040-25-9 Usage
Description
Δ2-Cefepime, also known as C242750, is a novel series of cephalosporins that are a class of β-lactam antibiotics. It is characterized by its brown solid appearance and possesses unique chemical properties that differentiate it from other cephalosporins.
Uses
Used in Pharmaceutical Industry:
Δ2-Cefepime is used as an antibiotic for the treatment of various bacterial infections. As a cephalosporin, it works by inhibiting bacterial cell wall synthesis, leading to bacterial cell death. Its unique chemical properties may provide advantages in terms of efficacy, safety, and resistance profile compared to other antibiotics in its class.
Additionally, research and development efforts may focus on exploring the potential of Δ2-Cefepime for specific applications, such as addressing antibiotic-resistant bacteria or targeting particular types of infections. Further studies would be required to determine its full range of uses and benefits in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 88040-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,4 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88040-25:
(7*8)+(6*8)+(5*0)+(4*4)+(3*0)+(2*2)+(1*5)=129
129 % 10 = 9
So 88040-25-9 is a valid CAS Registry Number.
88040-25-9Relevant articles and documents
Novel approach for the conversion of natural Δ3 cephalosporin derivatives into corresponding Δ2 cephalosporin derivatives
Prasada Rao, Korrapati V. V.,Dandala, Ramesh,Handa, Vijay K.,Kamat, Anand G.,Subramanyeswara Rao, Inti V.,Rani, Ananta,Naidu, Andra
, p. 1513 - 1515 (2008/09/18)
(Chemical Equation Presented) A simple one pot synthetic method for the isomerization of cephem double bond from the natural 3-position to 2-cephem positions is affected by silylation. Thus cephalosporin acids are treated with N-trimethylsilylacetamide (MSA) or N,O-bis(trimethylsilyl)acetamide (BSA) and the resulting silyl esters are treated with triethylamine at ambient temperature in the same pot to afford Δ2-cephalosporins, which are potentially related compounds in cephalosporin antibacterial compounds.
