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Avibactam

Base Information Edit
  • Chemical Name:Avibactam
  • CAS No.:1192500-31-4
  • Deprecated CAS:794508-22-8
  • Molecular Formula:C7H11N3O6S
  • Molecular Weight:265.247
  • Hs Code.:
  • UNII:7352665165,06MFO7817I
  • DSSTox Substance ID:DTXSID901026066
  • Nikkaji Number:J3.098.586I
  • Wikipedia:Avibactam
  • Wikidata:Q15410251
  • NCI Thesaurus Code:C171777
  • RXCUI:1603834
  • ChEMBL ID:CHEMBL1689063
  • Mol file:1192500-31-4.mol
Avibactam

Synonyms:avibactam;NXL 104;NXL-104;NXL104

Suppliers and Price of Avibactam
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
  • Crysdot
  • Avibactamfreeacid 98+%
  • 5mg
  • $ 168.00
  • Crysdot
  • Avibactamfreeacid 98+%
  • 50mg
  • $ 1050.00
  • Crysdot
  • Avibactamfreeacid 98+%
  • 10mg
  • $ 315.00
  • Chemenu
  • (1R,2S,5R)-2-carbamoyl-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-ylhydrogensulfate 98%
  • 10mg
  • $ 295.00
  • Chemenu
  • (1R,2S,5R)-2-carbamoyl-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-ylhydrogensulfate 98%
  • 50mg
  • $ 982.00
  • ApexBio Technology
  • Avibactam
  • 5mg
  • $ 537.00
  • American Custom Chemicals Corporation
  • AVIBACTAM 95.00%
  • 100MG
  • $ 995.00
  • American Custom Chemicals Corporation
  • AVIBACTAM 95.00%
  • 5MG
  • $ 499.80
Total 71 raw suppliers
Chemical Property of Avibactam Edit
Chemical Property:
  • PKA:-4.59±0.18(Predicted) 
  • PSA:139.61000 
  • Density:1.85 
  • LogP:0.58100 
  • XLogP3:-1.8
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:3
  • Exact Mass:265.03685625
  • Heavy Atom Count:17
  • Complexity:457
Purity/Quality:

99% *data from raw suppliers

Avibactamfreeacid 98+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC(N2CC1N(C2=O)OS(=O)(=O)O)C(=O)N
  • Isomeric SMILES:C1C[C@H](N2C[C@@H]1N(C2=O)OS(=O)(=O)O)C(=O)N
  • Recent ClinicalTrials:To Investigate the Safety and Tolerability of Aztreonam-Avibactam (ATM-AVI)
  • Recent EU Clinical Trials:A PROSPECTIVE, RANDOMIZED, OPEN-LABEL, COMPARATIVE STUDY TO ASSESS THE EFFICACY, SAFETY AND TOLERABILITY OF AZTREONAM-AVIBACTAM (ATM-AVI) AND BEST AVAILABLE THERAPY FOR THE TREATMENT OF SERIOUS INFECTIONS DUE TO MULTI-DRUG RESISTANT GRAM- NEGATIVE BACTERIA PRODUCING METALLO-Β-LACTAMASE (MBL)
Technology Process of Avibactam

There total 36 articles about Avibactam 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 chlorosulfonic acid; In N,N-dimethyl-formamide; at 30 ℃; for 48h; Reagent/catalyst;
Guidance literature:
(1R,2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamide; With hydrogen; 5% Pd-C; In dichloromethane; N,N-dimethyl-formamide; under 2250.23 Torr;
With sulfur trioxide-N,N-dimethylformamide complex; acetic acid; In dichloromethane; N,N-dimethyl-formamide;
Guidance literature:
With toluene-4-sulfonic acid; In dichloromethane; at 0 - 5 ℃; for 0.5h; Solvent; Reagent/catalyst; Temperature; Concentration;
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