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Penamecillin

Base Information
  • Chemical Name:Penamecillin
  • CAS No.:983-85-7
  • Molecular Formula:C19H22 N2 O6 S
  • Molecular Weight:406.459
  • Hs Code.:
  • European Community (EC) Number:213-571-8
  • UNII:H0P1YE5581
  • DSSTox Substance ID:DTXSID10243547
  • Nikkaji Number:J7.208G
  • Wikipedia:Penamecillin
  • Wikidata:Q7162195
  • NCI Thesaurus Code:C170307
  • Metabolomics Workbench ID:154522
  • ChEMBL ID:CHEMBL2106988
  • Mol file:983-85-7.mol
Penamecillin

Synonyms:benzylpenicillin acetoxymethyl ester;penamecillin

Suppliers and Price of Penamecillin
Supply Marketing:
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
  • PENAMECILLIN 95.00%
  • 5MG
  • $ 503.97
Total 5 raw suppliers
Chemical Property of Penamecillin
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:106-108° 
  • Boiling Point:648.8°Cat760mmHg 
  • Flash Point:346.2°C 
  • PSA:127.31000 
  • Density:1.37g/cm3 
  • LogP:1.16880 
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:8
  • Exact Mass:406.11985760
  • Heavy Atom Count:28
  • Complexity:661
Purity/Quality:

98%Min *data from raw suppliers

PENAMECILLIN 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)OCOC(=O)C1C(SC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)(C)C
  • Isomeric SMILES:CC(=O)OCOC(=O)[C@H]1C(S[C@H]2N1C(=O)[C@H]2NC(=O)CC3=CC=CC=C3)(C)C
  • Uses Antibacterial. Penamecillin is an ambulatory antibiotic used in the treatment of community-acquired pneumonia in adults. An antimicrobial agent also used in pharmacokinetics.
Technology Process of Penamecillin

There total 3 articles about Penamecillin 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:
In dimethyl sulfoxide; for 20h; Ambient temperature;
Guidance literature:
Benzylpenicillin, Brommethylacetat;
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