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viridicatin

Base Information
  • Chemical Name:viridicatin
  • CAS No.:129-24-8
  • Molecular Formula:C15H11 N O2
  • Molecular Weight:237.258
  • Hs Code.:2933499090
  • NSC Number:656625
  • UNII:45493KS618
  • DSSTox Substance ID:DTXSID10156022
  • Nikkaji Number:J5.422D
  • Wikidata:Q27258806
  • Metabolomics Workbench ID:164728
  • ChEMBL ID:CHEMBL2386742
  • Mol file:129-24-8.mol
viridicatin

Synonyms:Carbostyril,3-hydroxy-4-phenyl- (7CI,8CI); 2,3-Dihydroxy-4-phenylquinoline;2,6-Dihydroxy-4-phenylquinoline; 3-Hydroxy-4-phenyl-2(1H)-quinolinone;3-Hydroxy-4-phenyl-2-quinolone; 3-Hydroxy-4-phenylcarbostyril;3-Hydroxy-4-phenylquinolin-2-one; NSC 656625; Viridicatin; Viridicatine

Suppliers and Price of viridicatin
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
  • Usbiological
  • Viridicatin
  • 1mg
  • $ 426.00
  • TRC
  • Viridicatin
  • 25mg
  • $ 475.00
  • Cayman Chemical
  • Viridicatin ≥99%
  • 5mg
  • $ 470.00
  • Cayman Chemical
  • Viridicatin ≥99%
  • 1mg
  • $ 99.00
  • American Custom Chemicals Corporation
  • VIRIDICATIN 95.00%
  • 5MG
  • $ 496.84
  • AK Scientific
  • Viridicatin
  • 1mg
  • $ 233.00
Total 9 raw suppliers
Chemical Property of viridicatin
Chemical Property:
  • Vapor Pressure:6.79E-10mmHg at 25°C 
  • Melting Point:268° 
  • Boiling Point:476.7°Cat760mmHg 
  • Flash Point:242.1°C 
  • PSA:53.35000 
  • Density:1.323g/cm3 
  • LogP:3.31300 
  • XLogP3:2.4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:237.078978594
  • Heavy Atom Count:18
  • Complexity:369
Purity/Quality:

98%min *data from raw suppliers

Viridicatin *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C2=C(C(=O)NC3=CC=CC=C32)O
  • Uses Viridicatin is a fungal metabolite produced by several species of Penicillium and formed by the rearrangement of the benzodiazepine, cyclopenin. Viridicatin exhibits potent selective activity against Mycobacterium tuberculosis, but is inactive against most other bacteria. Viridicatin is a?Penicillium?metabolite active against?Mycobacterium tuberculosis. Isolated from deep-sea Penicillium griseofulvum alleviates anaphylaxis and has anti-?allergic properties.
Technology Process of viridicatin

There total 27 articles about viridicatin 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:
2,2-dichloro-N-(4-methoxybenzyl)-N-phenylacetamide; benzaldehyde; With potassium tert-butylate; In toluene; at -45 - 20 ℃; for 6.5h;
With hydrogenchloride; In toluene; Cooling with ice;
DOI:10.1021/acs.joc.1c01592
Guidance literature:
With potassium carbonate; toluene-4-sulfonic acid hydrazide; In ethanol; at 80 ℃; for 8h; Reagent/catalyst; Solvent; Temperature; regioselective reaction;
DOI:10.1021/acs.orglett.8b01417
Guidance literature:
With sulfuric acid; at 20 ℃; for 1h; Cooling with ice;
DOI:10.1002/hlca.201300074
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