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Technology Process of Urea, N-(bis(1-aziridinyl)phosphinyl)-N'-(2,4-dichlorophenyl)-

Urea, N-(bis(1-aziridinyl)phosphinyl)-N'-(2,4-dichlorophenyl)-

Base Information
  • Chemical Name:Urea, N-(bis(1-aziridinyl)phosphinyl)-N'-(2,4-dichlorophenyl)-
  • CAS No.:4797-24-4
  • Molecular Formula:C11H13Cl2N4O2P
  • Molecular Weight:335.1263
  • Hs Code.:
  • UNII:3SZG7T8ZP6
  • DSSTox Substance ID:DTXSID70197370
  • Wikidata:Q83070262
  • Mol file:4797-24-4.mol
Urea, N-(bis(1-aziridinyl)phosphinyl)-N'-(2,4-dichlorophenyl)-

Synonyms:4797-24-4;Urea, N-(bis(1-aziridinyl)phosphinyl)-N'-(2,4-dichlorophenyl)-;N-(Bis(1-aziridinyl)phosphinyl)-N'-(2,4-dichlorophenyl)urea;3SZG7T8ZP6;Urea, 1-(bis(1-aziridinyl)phosphinyl)-3-(2,4-dichlorophenyl)-;UNII-3SZG7T8ZP6;DTXSID70197370;1-(BIS(AZIRIDIN-1-YL)PHOSPHORYL)-3-(2,4-DICHLOROPHENYL)UREA;BIS(1-AZIRIDINYL)PHOSPHINYL)-N'-(2,4-DICHLOROPHENYL)UREA, N-(

Suppliers and Price of Urea, N-(bis(1-aziridinyl)phosphinyl)-N'-(2,4-dichlorophenyl)-
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
  • American Custom Chemicals Corporation
  • UREA, 1-(BIS(1-AZIRIDINYL)PHOSPHINYL)-3-(2,4-DICHLOROPHENYL)- 95.00%
  • 5MG
  • $ 500.91
Total 0 raw suppliers
Chemical Property of Urea, N-(bis(1-aziridinyl)phosphinyl)-N'-(2,4-dichlorophenyl)-
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • PKA:11.29±0.20(Predicted) 
  • Flash Point:°C 
  • PSA：74.03000 
  • Density:1.61g/cm3 
  • LogP:3.19390 
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:334.0153181
  • Heavy Atom Count:20
  • Complexity:428
Purity/Quality:

UREA, 1-(BIS(1-AZIRIDINYL)PHOSPHINYL)-3-(2,4-DICHLOROPHENYL)- 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CN1P(=O)(NC(=O)NC2=C(C=C(C=C2)Cl)Cl)N3CC3
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