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1-(2-Isocyanophenyl)pyrrole

Base Information Edit
  • Chemical Name:1-(2-Isocyanophenyl)pyrrole
  • CAS No.:350829-07-1
  • Molecular Formula:C11H8N2
  • Molecular Weight:168.198
  • Hs Code.:2933990090
  • DSSTox Substance ID:DTXSID20377746
  • Nikkaji Number:J961.100B
  • Wikidata:Q82167091
  • Mol file:350829-07-1.mol
1-(2-Isocyanophenyl)pyrrole

Synonyms:1-(2-isocyanophenyl)pyrrole;350829-07-1;SCHEMBL2560232;2-(1-Pyrrolyl)phenyl isocyanide;DTXSID20377746;AKOS006344277;FT-0705977

Suppliers and Price of 1-(2-Isocyanophenyl)pyrrole
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
  • Packaging
  • price
  • CHESS?
  • PN100339:1-(2-Isocyanophenyl)pyrrole 95
  • 5 g
  • $ 1056.00
Total 5 raw suppliers
Chemical Property of 1-(2-Isocyanophenyl)pyrrole Edit
Chemical Property:
  • PSA:4.93000 
  • LogP:2.25880 
  • XLogP3:2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:168.068748264
  • Heavy Atom Count:13
  • Complexity:209
Purity/Quality:

98% *data from raw suppliers

PN100339:1-(2-Isocyanophenyl)pyrrole 95 *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:[C-]#[N+]C1=CC=CC=C1N2C=CC=C2
Technology Process of 1-(2-Isocyanophenyl)pyrrole

There total 3 articles about 1-(2-Isocyanophenyl)pyrrole 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:
With triethylamine; trichlorophosphate; In tetrahydrofuran; at 0 ℃;
DOI:10.1246/cl.1998.551
Guidance literature:
Multi-step reaction with 2 steps
1: 70 percent / 216 h / Heating
2: 78 percent / triethylamine; phosphoryl chloride / tetrahydrofuran / 0.2 h / 0 °C
With triethylamine; trichlorophosphate; In tetrahydrofuran;
DOI:10.1246/bcsj.74.1109
Guidance literature:
Multi-step reaction with 3 steps
1: copper(l) iodide; potassium phosphate; N,N-dimethylethylenediamine / toluene / 24 h / 110 °C / Inert atmosphere
2: tetrahydrofuran / 0.5 h / 0 - 20 °C
3: trichlorophosphate; triethylamine / tetrahydrofuran / 4 h / 0 °C
With potassium phosphate; copper(l) iodide; N,N-dimethylethylenediamine; triethylamine; trichlorophosphate; In tetrahydrofuran; toluene;
DOI:10.1021/acs.orglett.7b00375
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