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Technology Process of 1-(2,5-Dichlorophenyl)-3-(4-(morpholino)phenyl)-5-(m-nitrobenzylidene)thiobarbituric acid

1-(2,5-Dichlorophenyl)-3-(4-(morpholino)phenyl)-5-(m-nitrobenzylidene)thiobarbituric acid

Base Information
  • Chemical Name:1-(2,5-Dichlorophenyl)-3-(4-(morpholino)phenyl)-5-(m-nitrobenzylidene)thiobarbituric acid
  • CAS No.:121608-34-2
  • Molecular Formula:C27H20 Cl2 N4 O5 S
  • Molecular Weight:583.44
  • Hs Code.:
  • Wikidata:Q76389712
  • Mol file:121608-34-2.mol
1-(2,5-Dichlorophenyl)-3-(4-(morpholino)phenyl)-5-(m-nitrobenzylidene)thiobarbituric acid

Synonyms:121608-34-2;1-(2,5-Dichlorophenyl)-3-(4-(morpholino)phenyl)-5-(m-nitrobenzylidene)thiobarbituric acid;(5Z)-1-(2,5-dichlorophenyl)-3-(4-morpholin-4-ylphenyl)-5-[(3-nitrophenyl)methylidene]-2-sulfanylidene-1,3-diazinane-4,6-dione;1-(2,5-dichlorophenyl)-3-(4-morpholin-4-ylphenyl)-5-[(3-nitrophenyl)methylidene]-2-sulfanylidene-1,3-diazinane-4,6-dione;4,6(1H,5H)-Pyrimidinedione, dihydro-1-(2,5-dichlorophenyl)-3-(4-(4-morpholinyl)phenyl)-5-((3-nitrophenyl)methylene)-2-thioxo-;LS-135233

Suppliers and Price of 1-(2,5-Dichlorophenyl)-3-(4-(morpholino)phenyl)-5-(m-nitrobenzylidene)thiobarbituric acid
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 1-(2,5-Dichlorophenyl)-3-(4-(morpholino)phenyl)-5-(m-nitrobenzylidene)thiobarbituric acid
Chemical Property:
  • Vapor Pressure:2.05E-22mmHg at 25°C 
  • Boiling Point:750.7°Cat760mmHg 
  • PKA:3.59±0.40(Predicted) 
  • Flash Point:407.8°C 
  • PSA：131.00000 
  • Density:1.58g/cm3 
  • LogP:6.20470 
  • XLogP3:5.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:4
  • Exact Mass:582.0531463
  • Heavy Atom Count:39
  • Complexity:995
Purity/Quality:
Safty Information:
  • Pictogram(s):  
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MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1COCCN1C2=CC=C(C=C2)N3C(=O)C(=CC4=CC(=CC=C4)[N+](=O)[O-])C(=O)N(C3=S)C5=C(C=CC(=C5)Cl)Cl
  • Isomeric SMILES:C1COCCN1C2=CC=C(C=C2)N3C(=O)/C(=C/C4=CC(=CC=C4)[N+](=O)[O-])/C(=O)N(C3=S)C5=C(C=CC(=C5)Cl)Cl
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