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Encyclopedia

Ceftolozane

Base Information Edit
  • Chemical Name:Ceftolozane
  • CAS No.:689293-68-3
  • Molecular Formula:C23H30N12O8S2
  • Molecular Weight:666.699
  • Hs Code.:
  • UNII:37A4IES95Q
  • DSSTox Substance ID:DTXSID901031217
  • Wikipedia:Ceftolozane/tazobactam
  • NCI Thesaurus Code:C150024
  • RXCUI:1597609
  • Metabolomics Workbench ID:152110
  • Mol file:689293-68-3.mol
Ceftolozane

Synonyms:ceftolozane;ceftolozane sulfate;CXA-101;FR 264205;FR-264205;FR26 4205;FR264205

Suppliers and Price of Ceftolozane
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
  • American Custom Chemicals Corporation
  • CEFTOLOZANE 95.00%
  • 5MG
  • $ 504.58
Total 19 raw suppliers
Chemical Property of Ceftolozane Edit
Chemical Property:
  • XLogP3:-3.2
  • Hydrogen Bond Donor Count:7
  • Hydrogen Bond Acceptor Count:16
  • Rotatable Bond Count:11
  • Exact Mass:666.17509831
  • Heavy Atom Count:45
  • Complexity:1280
Purity/Quality:

99% *data from raw suppliers

CEFTOLOZANE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C)(C(=O)O)ON=C(C1=NSC(=N1)N)C(=O)NC2C3N(C2=O)C(=C(CS3)C[N+]4=CC(=C(N4C)N)NC(=O)NCCN)C(=O)[O-]
  • Isomeric SMILES:CC(C)(C(=O)O)O/N=C(/C1=NSC(=N1)N)\C(=O)N[C@H]2[C@@H]3N(C2=O)C(=C(CS3)C[N+]4=CC(=C(N4C)N)NC(=O)NCCN)C(=O)[O-]
  • Recent ClinicalTrials:Comparative Study To Determine The Efficacy, Safety, And Tolerability Of Ceftolozane-Tazobactam
  • Recent EU Clinical Trials:Intrapulmonary penetration of ceftolozane / tazobactam and ceftazidime / avibactam administered in continuous infusion in critically ill patients with nosocomial pneumonia
  • Uses Ceftolozane Sulfate is an antibiotic belonging to the class of Cephalosporin (Cephalosporin C Zinc Salt, C258750).
Technology Process of Ceftolozane

There total 10 articles about Ceftolozane 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 ammonium hydroxide; In water; at 10 ℃; for 0.5h; pH=6.5;
Guidance literature:
With trichloroacetic acid; In phenol; at 25 - 35 ℃; for 1h; Inert atmosphere;
Guidance literature:
With trichloroacetic acid; In phenol; at 35 - 45 ℃; for 1.5h; Inert atmosphere;
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