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Technology Process of N',N'-dimethyl-N-[5-[(E)-2-(5-nitrofuran-2-yl)ethenyl]-1,3,4-oxadiazol-2-yl]methanediamine

N',N'-dimethyl-N-[5-[(E)-2-(5-nitrofuran-2-yl)ethenyl]-1,3,4-oxadiazol-2-yl]methanediamine

Base Information
  • Chemical Name:N',N'-dimethyl-N-[5-[(E)-2-(5-nitrofuran-2-yl)ethenyl]-1,3,4-oxadiazol-2-yl]methanediamine
  • CAS No.:55738-54-0
  • Molecular Formula:C11H11 N5 O4
  • Molecular Weight:277.27
  • Hs Code.:
  • DSSTox Substance ID:DTXSID7020502
  • ChEMBL ID:CHEMBL265931
  • Mol file:55738-54-0.mol
N',N'-dimethyl-N-[5-[(E)-2-(5-nitrofuran-2-yl)ethenyl]-1,3,4-oxadiazol-2-yl]methanediamine

Synonyms:CHEMBL265931;DTXSID7020502;Q63088197

Suppliers and Price of N',N'-dimethyl-N-[5-[(E)-2-(5-nitrofuran-2-yl)ethenyl]-1,3,4-oxadiazol-2-yl]methanediamine
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
  • TRANS-2-((DIMETHYLAMINO)METHYLIMINO)-5-(2-(5-NITRO-2-FURYL)VINYL)-1,3,4-OXADIAZOLE) 95.00%
  • 5MG
  • $ 504.77
Total 4 raw suppliers
Chemical Property of N',N'-dimethyl-N-[5-[(E)-2-(5-nitrofuran-2-yl)ethenyl]-1,3,4-oxadiazol-2-yl]methanediamine
Chemical Property:
  • Refractive Index:1.7000 (estimate) 
  • Boiling Point:424.9°Cat760mmHg 
  • PKA:2.00±0.50(Predicted) 
  • Flash Point:210.8°C 
  • PSA：113.15000 
  • Density:1.422g/cm3 
  • LogP:2.26840 
  • XLogP3:1.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:5
  • Exact Mass:279.09675391
  • Heavy Atom Count:20
  • Complexity:359
Purity/Quality:

99% *data from raw suppliers

TRANS-2-((DIMETHYLAMINO)METHYLIMINO)-5-(2-(5-NITRO-2-FURYL)VINYL)-1,3,4-OXADIAZOLE) 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CN(C)CNC1=NN=C(O1)C=CC2=CC=C(O2)[N+](=O)[O-]
  • Isomeric SMILES:CN(C)CNC1=NN=C(O1)/C=C/C2=CC=C(O2)[N+](=O)[O-]
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