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Chloramphenicol 1-acetate

Base Information
  • Chemical Name:Chloramphenicol 1-acetate
  • CAS No.:23214-93-9
  • Molecular Formula:C13H14Cl2N2O6
  • Molecular Weight:365.17
  • Hs Code.:2924299090
  • DSSTox Substance ID:DTXSID10945897
  • Nikkaji Number:J1.692.372I
  • Wikidata:Q82923358
  • ChEMBL ID:CHEMBL4160785
  • Mol file:23214-93-9.mol
Chloramphenicol 1-acetate

Synonyms:1-acetylchloramphenicol;chloramphenicol 1-acetate

Suppliers and Price of Chloramphenicol 1-acetate
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
  • TRC
  • Chloramphenicol1-Acetate
  • 10mg
  • $ 545.00
  • Biosynth Carbosynth
  • Chloramphenicol 1-acetate
  • 5 mg
  • $ 495.50
  • Biosynth Carbosynth
  • Chloramphenicol 1-acetate
  • 2 mg
  • $ 272.60
  • Biosynth Carbosynth
  • Chloramphenicol 1-acetate
  • 1 mg
  • $ 149.90
  • Biosynth Carbosynth
  • Chloramphenicol 1-acetate
  • 25 mg
  • $ 1638.00
  • Biosynth Carbosynth
  • Chloramphenicol 1-acetate
  • 10 mg
  • $ 900.90
  • AK Scientific
  • Chloramphenicol1-acetate
  • 5mg
  • $ 718.00
Total 5 raw suppliers
Chemical Property of Chloramphenicol 1-acetate
Chemical Property:
  • Vapor Pressure:8.32E-14mmHg at 25°C 
  • Refractive Index:1.576 
  • Boiling Point:569.5°Cat760mmHg 
  • Flash Point:298.2°C 
  • PSA:121.45000 
  • Density:1.473g/cm3 
  • LogP:2.39390 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Chloroform (Slightly), Ethyl Acetate, Methanol (Slightly) 
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:7
  • Exact Mass:364.0228916
  • Heavy Atom Count:23
  • Complexity:435
Purity/Quality:

97% *data from raw suppliers

Chloramphenicol1-Acetate *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)OC(C1=CC=C(C=C1)[N+](=O)[O-])C(CO)NC(=O)C(Cl)Cl
  • Isomeric SMILES:CC(=O)O[C@H](C1=CC=C(C=C1)[N+](=O)[O-])[C@@H](CO)NC(=O)C(Cl)Cl
  • Uses Found in the metabolic decomposition of Chloramphenicol by Alcaligenes faecalis. A Chloramphenicol (C325030) derivative.
Technology Process of Chloramphenicol 1-acetate

There total 1 articles about Chloramphenicol 1-acetate 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:
Chloramphenicol, Streptomyces coelicolor;
DOI:10.7164/antibiotics.24.206
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