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LISTERIA MOX SUPPLEMENT

Base Information Edit
  • Chemical Name:LISTERIA MOX SUPPLEMENT
  • CAS No.:75007-71-5
  • Molecular Formula:C20H20N6O9S
  • Molecular Weight:520.48
  • Hs Code.:
  • Mol file:75007-71-5.mol
LISTERIA MOX SUPPLEMENT

Synonyms:

Suppliers and Price of LISTERIA MOX SUPPLEMENT
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 1 raw suppliers
Chemical Property of LISTERIA MOX SUPPLEMENT Edit
Chemical Property:
  • PKA:pKa 2.4(H2O) (Uncertain);3.5 (Uncertain) 
  • Storage Temp.:2-8°C 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Description As was already stated, and which is visible from the scheme of synthesis, moxalactam contains a dihydrooxazine ring instead of the dihydrothiazine ring common to all cephalosporins, and thus this compound cannot be formally numbered with cephalosporins, cephamicins, or penicillins; however, in terms of pharmacological action, it is related to all three of the antibiotics listed above, and it is classified as a third-generation cephalosporin. Moxalactam is resistant to the action of beta-lactamase, penicillinase, and cephalosporinase, which are produced by Gram-negative and Gram-positive bacteria. Many strains of a number of microorganisms that possess multiple resistance to other antibiotics— semisynthetic penicillins, cephalosporins, and aminoglycosides—are sensitive to moxalactam. This drug is used for infections of the respiratory organs, urinal tract, abdominal cavity, as well as for gynecological infections, infections of the bones, joints, skin, soft tissues, and for gonorrhea. Synonyms of this drug are latamoxef, festamoxin, moxacef, moxam, and many others.
Technology Process of LISTERIA MOX SUPPLEMENT

There total 20 articles about LISTERIA MOX SUPPLEMENT which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With trichloroacetic acid; In phenol; at 25 - 35 ℃; for 1.5h; Temperature; Solvent; Inert atmosphere;
Guidance literature:
With trichloroacetic acid; In phenol; at 25 - 35 ℃; for 2.5h; Solvent; Temperature; Inert atmosphere;
Guidance literature:
With trichloroacetic acid; In phenol; at 25 - 35 ℃; for 2h; Solvent; Temperature; Inert atmosphere;
Refernces Edit
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