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N-Isobutyl-5-nitro-2-furylacrylamide

Base Information
  • Chemical Name:N-Isobutyl-5-nitro-2-furylacrylamide
  • CAS No.:89811-25-6
  • Molecular Formula:C11H14N2O4
  • Molecular Weight:238.243
  • Hs Code.:
N-Isobutyl-5-nitro-2-furylacrylamide

Synonyms:N-Isobutyl-5-nitro-2-furanacrylamide;CCRIS 5649;89811-25-6;N-Isobutyl-5-nitro-2-furylacrylamide;BRN 0019013;N-(2-Methylpropyl)-3-(5-nitro-2-furanyl)-2-propenamide;2-Propenamide, N-(2-methylpropyl)-3-(5-nitro-2-furanyl)-

Suppliers and Price of N-Isobutyl-5-nitro-2-furylacrylamide
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Chemical Property of N-Isobutyl-5-nitro-2-furylacrylamide
Chemical Property:
  • Vapor Pressure:1.67E-07mmHg at 25°C 
  • Boiling Point:427.2°Cat760mmHg 
  • Flash Point:212.2°C 
  • Density:1.206g/cm3 
  • XLogP3:2.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:238.09535693
  • Heavy Atom Count:17
  • Complexity:309
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)CNC(=O)C=CC1=CC=C(O1)[N+](=O)[O-]
Technology Process of N-Isobutyl-5-nitro-2-furylacrylamide

There total 3 articles about N-Isobutyl-5-nitro-2-furylacrylamide 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:
Multi-step reaction with 3 steps
1: nitric acid; acetic anhydride / -15 - -5 °C
2: thionyl chloride / benzene / 4 h / Heating
3: 67.5 percent / benzene / 24 h / 20 °C
With thionyl chloride; nitric acid; acetic anhydride; In benzene;
DOI:10.1016/j.bmcl.2005.01.002
Guidance literature:
Multi-step reaction with 2 steps
1: thionyl chloride / benzene / 4 h / Heating
2: 67.5 percent / benzene / 24 h / 20 °C
With thionyl chloride; In benzene;
DOI:10.1016/j.bmcl.2005.01.002
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