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D-Urobilinogen

Base Information
  • Chemical Name:D-Urobilinogen
  • CAS No.:17208-65-0
  • Molecular Formula:C33H42 N4 O6
  • Molecular Weight:0
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20331525,DTXSID60864746
  • Wikidata:Q27106322
  • Metabolomics Workbench ID:38481
  • Mol file:17208-65-0.mol
D-Urobilinogen

Synonyms:D-Urobilinogen;17208-65-0;3-(2-{[3-(2-carboxyethyl)-5-[(4-ethenyl-3-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-yl)methyl]-4-methyl-1H-pyrrol-2-yl]methyl}-5-[(3-ethyl-4-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-yl)methyl]-4-methyl-1H-pyrrol-3-yl)propanoic acid;3-{2-({3-(2-Carboxyethyl)-5-[(4-ethenyl-3-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-yl)methyl]-4-methyl-1H-pyrrol-2-yl}methyl)-5-[(3-ethyl-4-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-yl)methyl]-4-methyl-1H-pyrrol-3-yl}propanoic acid;C05791;3-[2-[[3-(2-carboxyethyl)-5-[(3-ethyl-4-methyl-5-oxo-1,2-dihydropyrrol-2-yl)methyl]-4-methyl-1H-pyrrol-2-yl]methyl]-5-[(4-ethenyl-3-methyl-5-oxo-1,2-dihydropyrrol-2-yl)methyl]-4-methyl-1H-pyrrol-3-yl]propanoic acid;CHEBI:4260;DTXSID20331525;DTXSID60864746;Q27106322;3-[2-[[3-(2-carboxyethyl)-5-[(4-ethenyl-3-methyl-5-oxo-1,2-dihydropyrrol-2-yl)methyl]-4-methyl-1H-py

Suppliers and Price of D-Urobilinogen
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
Total 2 raw suppliers
Chemical Property of D-Urobilinogen
Chemical Property:
  • Vapor Pressure:2.92E-33mmHg at 25°C 
  • Boiling Point:881.3°Cat760mmHg 
  • Flash Point:486.8°C 
  • PSA:171.36000 
  • Density:1.275g/cm3 
  • LogP:4.44740 
  • XLogP3:2.7
  • Hydrogen Bond Donor Count:6
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:14
  • Exact Mass:590.31043507
  • Heavy Atom Count:43
  • Complexity:1190
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC1=C(C(=O)NC1CC2=C(C(=C(N2)CC3=C(C(=C(N3)CC4C(=C(C(=O)N4)C=C)C)C)CCC(=O)O)CCC(=O)O)C)C
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