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Cefteram pivoxil

Base Information Edit
  • Chemical Name:Cefteram pivoxil
  • CAS No.:82547-81-7
  • Molecular Formula:C22H27N9O7S2
  • Molecular Weight:593.64
  • Hs Code.:
  • UNII:0OD86RT58C
  • DSSTox Substance ID:DTXSID401316612
  • Nikkaji Number:J269.593F
  • NCI Thesaurus Code:C98230
  • ChEMBL ID:CHEMBL3137676
  • Mol file:82547-81-7.mol
Cefteram pivoxil

Synonyms:cefteram pivoxil;Ro 19-5248;Ro-19-5248;T 2588;T-2588;Tomiron

Suppliers and Price of Cefteram pivoxil
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
  • CefteramPivoxil
  • 25mg
  • $ 460.00
  • Medical Isotopes, Inc.
  • CefteramPivoxil
  • 10 mg
  • $ 650.00
  • Biosynth Carbosynth
  • Cefteram pivoxil
  • 10 mg
  • $ 300.00
  • Biosynth Carbosynth
  • Cefteram pivoxil
  • 5 mg
  • $ 187.50
  • Biosynth Carbosynth
  • Cefteram pivoxil
  • 2 mg
  • $ 95.00
  • Biosynth Carbosynth
  • Cefteram pivoxil
  • 1 mg
  • $ 60.00
  • Biosynth Carbosynth
  • Cefteram pivoxil
  • 25 mg
  • $ 637.50
  • American Custom Chemicals Corporation
  • CEFTERAM PIVOXIL 95.00%
  • 10MG
  • $ 1963.50
  • American Custom Chemicals Corporation
  • CEFTERAM PIVOXIL 95.00%
  • 1MG
  • $ 750.75
Total 53 raw suppliers
Chemical Property of Cefteram pivoxil Edit
Chemical Property:
  • Melting Point:125-128 °C 
  • Refractive Index:1.744 
  • PKA:8.08±0.60(Predicted) 
  • PSA:259.65000 
  • Density:1.662 g/cm3 
  • LogP:0.72490 
  • Storage Temp.:Hygroscopic, -20°C Freezer, Under Inert Atmosphere 
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:15
  • Rotatable Bond Count:12
  • Exact Mass:593.14748658
  • Heavy Atom Count:40
  • Complexity:1100
Purity/Quality:

CefteramPivoxil *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=NN(N=N1)CC2=C(N3C(C(C3=O)NC(=O)C(=NOC)C4=CSC(=N4)N)SC2)C(=O)OCOC(=O)C(C)(C)C
  • Isomeric SMILES:CC1=NN(N=N1)CC2=C(N3[C@@H]([C@@H](C3=O)NC(=O)/C(=N\OC)/C4=CSC(=N4)N)SC2)C(=O)OCOC(=O)C(C)(C)C
  • Uses Third generation, orally active cephalosporin antibiotic. Antibacterial.
Technology Process of Cefteram pivoxil

There total 5 articles about Cefteram pivoxil 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:
C21H25N9O7S2; With tetrapropylammonium iodide; In 1,4-dioxane; at 20 ℃; for 2h;
iodomethyl pivaloate; With pyridine; In 1,4-dioxane; at -10 - 20 ℃; for 1h;
With t-butyldimethylsiyl triflate; In 1,4-dioxane; at 0 ℃; for 0.25h;
Guidance literature:
cefteram; With sodium methylate; In methanol; N,N-dimethyl-formamide; at -20 ℃; for 0.333333h;
iodomethyl pivaloate; In methanol; N,N-dimethyl-formamide; at -20 ℃; for 2.5h;
Guidance literature:
Multi-step reaction with 3 steps
1.1: sulfuric acid / 0.33 h / 20 °C
1.2: 20 °C
2.1: dichloromethane / 2 h / 20 °C
2.2: 0.5 h / 20 °C
3.1: tetrapropylammonium iodide / 1,4-dioxane / 2 h / 20 °C
3.2: 1 h / -10 - 20 °C
3.3: 0.25 h / 0 °C
With sulfuric acid; tetrapropylammonium iodide; In 1,4-dioxane; dichloromethane;
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