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4-(Benzylamino)-1-methyl-1H-imidazole-5-carboxamide

Base Information Edit
  • Chemical Name:4-(Benzylamino)-1-methyl-1H-imidazole-5-carboxamide
  • CAS No.:64995-66-0
  • Molecular Formula:C12H14N4O
  • Molecular Weight:230.269
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10553991
  • Wikidata:Q82434766
  • Mol file:64995-66-0.mol
4-(Benzylamino)-1-methyl-1H-imidazole-5-carboxamide

Synonyms:64995-66-0;4-(Benzylamino)-1-methyl-1H-imidazole-5-carboxamide;DTXSID10553991

Suppliers and Price of 4-(Benzylamino)-1-methyl-1H-imidazole-5-carboxamide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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Total 0 raw suppliers
Chemical Property of 4-(Benzylamino)-1-methyl-1H-imidazole-5-carboxamide Edit
Chemical Property:
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:230.11676108
  • Heavy Atom Count:17
  • Complexity:265
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CN1C=NC(=C1C(=O)N)NCC2=CC=CC=C2
Technology Process of 4-(Benzylamino)-1-methyl-1H-imidazole-5-carboxamide

There total 2 articles about 4-(Benzylamino)-1-methyl-1H-imidazole-5-carboxamide 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:
1.Prep. Sulfonat VI, NaOH;
Guidance literature:
Multi-step reaction with 4 steps
1: aq. AcOH-AcONa buffer, 10 percent aq. NaOH / ethyl acetate / 3.5 h / Ambient temperature; pH 5.2-5.3
2: 0.5 N aq. NaOH / 0.17 h / Heating
3: 1.) K2CO3 / 1.) DMF, 80 deg C, 1 h, 2.) room temperature, 3 h
4: 70 percent / H2, 70percent aq. HClO4 / 10percent Pd/C / acetic acid / 760 Torr / 1.) 40 deg C, 4 h, 2.) 60 deg C, 13 h
With sodium hydroxide; perchloric acid; AcOH-AcONa buffer; hydrogen; potassium carbonate; palladium on activated charcoal; In acetic acid; ethyl acetate;
DOI:10.1248/cpb.39.2855
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