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Faropenem

Base Information Edit
  • Chemical Name:Faropenem
  • CAS No.:106560-14-9
  • Molecular Formula:C12H15NO5S
  • Molecular Weight:285.321
  • Hs Code.:
  • UNII:F52Y83BGH3
  • DSSTox Substance ID:DTXSID0046430
  • Nikkaji Number:J550.682D
  • Wikipedia:Faropenem
  • Wikidata:Q1397045
  • NCI Thesaurus Code:C72776
  • Metabolomics Workbench ID:49607
  • ChEMBL ID:CHEMBL556262
  • Mol file:106560-14-9.mol
Faropenem

Synonyms:(5R,6S)-6-(R)-1-hydroxyethyl-7-oxo-3-(R)-2-tetrahydrofuryl-4-thia-1-azabicyclo(3.2.0)hept-2-ene-2-carboxylate;faropenem;fropenem

Suppliers and Price of Faropenem
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
  • TRC
  • Faropenem
  • 100mg
  • $ 580.00
  • AvaChem
  • Faropenem
  • 1g
  • $ 279.00
  • AvaChem
  • Faropenem
  • 100mg
  • $ 89.00
  • AvaChem
  • Faropenem
  • 10mg
  • $ 39.00
  • American Custom Chemicals Corporation
  • FROPENEM 95.00%
  • 5G
  • $ 927.76
  • AHH
  • Fropenem 98%
  • 100mg
  • $ 600.00
Total 96 raw suppliers
Chemical Property of Faropenem Edit
Chemical Property:
  • Appearance/Colour:Light yellow powder 
  • Vapor Pressure:2.23E-15mmHg at 25°C 
  • Refractive Index:1.668 
  • Boiling Point:570.249 °C at 760 mmHg 
  • PKA:4.00±0.40(Predicted) 
  • Flash Point:298.676 °C 
  • PSA:112.37000 
  • Density:1.569 g/cm3 
  • LogP:0.31160 
  • XLogP3:0.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:3
  • Exact Mass:285.06709375
  • Heavy Atom Count:19
  • Complexity:477
Purity/Quality:

98%,99%, *data from raw suppliers

Faropenem *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C1C2N(C1=O)C(=C(S2)C3CCCO3)C(=O)O)O
  • Isomeric SMILES:C[C@H]([C@@H]1[C@@H]2N(C1=O)C(=C(S2)[C@H]3CCCO3)C(=O)O)O
  • Recent ClinicalTrials:Trial of Faropenem and Cefadroxil (in Combination With Amoxicillin/Clavulanic Acid and Standard TB Drugs) in Patients With Pulmonary Tuberculosis: Measurement of Early Bactericidal Activity and Effects on Novel Biomarkers
  • Recent NIPH Clinical Trials:Verification of the effectiveness of the combination therapy with an oral antibiotics and Adapalene for the treatment of acne vulgaris.
  • Description Farom was launched in Japan for use as an antibiotic against common respiratory tract pathogens. It can be prepared by several related routes of about seven steps starting with tetrahydrofuran-2-thiocarboxylic acid and a silylated azetidinone. It is a broad spectrum oral penem antibiotic that is β-lactamase stable. Farom is the most active β-lactam against anaerobes (more than cefaclor, cefixime and amoxicillin) but also has activity against Gram-positive, Gram-negative and enterobacteriaceae. It is equally active against strains carrying plasmid and chromosome mediated β-lactamases. The short plasma elimination half-life is the result of hydrolysis by renal dehydropeptidase. It is more stable to hydrolysis by extended spectrum β-lactamases than some second and third generation cephalosporins.
  • Uses Faropenem (cas# 106560-14-9) is a compound useful in organic synthesis. Treatmentof bacterial infections.
Technology Process of Faropenem

There total 6 articles about Faropenem 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 hydrogenchloride; palladium on activated charcoal; hydrogen; In methanol; at 40 ℃; for 16h; under 3040.2 Torr;
Guidance literature:
(5R,6S)-6-[1(R)-hydroxyethyl]-2-[2(R)-tetrahydrofuryl]penem-3-carboxylic acid 4-nitrobenzyl ester; With hydrogen; sodium hydrogencarbonate; 5%-palladium/activated carbon; In water; ethyl acetate; at 20 - 30 ℃; under 4413.43 - 5149.01 Torr;
With hydrogenchloride; In water; for 1h; pH=1.8 - 2.0; Product distribution / selectivity;
Guidance literature:
Multi-step reaction with 4 steps
1: sodium hydroxide / acetone / 2 h / 0 - 20 °C / pH 8 - 10
2: triethylamine / dichloromethane / 2 h / 0 - 5 °C
3: triethyl phosphite / 5,5-dimethyl-1,3-cyclohexadiene / 5 h / Reflux
4: hydrogenchloride; palladium on activated charcoal; hydrogen / methanol / 16 h / 40 °C / 3040.2 Torr
With hydrogenchloride; palladium on activated charcoal; hydrogen; triethylamine; sodium hydroxide; triethyl phosphite; In methanol; 5,5-dimethyl-1,3-cyclohexadiene; dichloromethane; acetone;
Refernces Edit
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