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Indolizine-2-carbonitrile

Base Information
  • Chemical Name:Indolizine-2-carbonitrile
  • CAS No.:153274-67-0
  • Molecular Formula:C9H6 N2
  • Molecular Weight:142.16
  • Hs Code.:
  • European Community (EC) Number:865-340-1
  • DSSTox Substance ID:DTXSID80700930
  • Nikkaji Number:J2.041.575D
  • Wikidata:Q82632442
  • Mol file:153274-67-0.mol
Indolizine-2-carbonitrile

Synonyms:INDOLIZINE-2-CARBONITRILE;153274-67-0;2-Indolizinecarbonitrile;2-cyanoindolizine;SCHEMBL1994209;DTXSID80700930;LOQCUYOSKCAMJF-UHFFFAOYSA-N;AKOS026729824;CS-0261396;EN300-78381;Z1203730717

Suppliers and Price of Indolizine-2-carbonitrile
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
  • TRC
  • indolizine-2-carbonitrile
  • 250mg
  • $ 310.00
  • American Custom Chemicals Corporation
  • INDOLIZINE-2-CARBONITRILE 95.00%
  • 5MG
  • $ 502.34
  • AK Scientific
  • Indolizine-2-carbonitrile
  • 5g
  • $ 1269.00
  • AK Scientific
  • Indolizine-2-carbonitrile
  • 1g
  • $ 503.00
Total 6 raw suppliers
Chemical Property of Indolizine-2-carbonitrile
Chemical Property:
  • PSA:28.20000 
  • LogP:1.81098 
  • XLogP3:2.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:142.053098200
  • Heavy Atom Count:11
  • Complexity:191
Purity/Quality:

99% *data from raw suppliers

indolizine-2-carbonitrile *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC2=CC(=CN2C=C1)C#N
Technology Process of Indolizine-2-carbonitrile

There total 3 articles about Indolizine-2-carbonitrile 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:
In 2,2,2-trifluoroethanol; at 100 ℃; for 1h; Time; Solvent; Microwave irradiation;
DOI:10.5935/0103-5053.20130056
Guidance literature:
at 120 ℃; for 1h;
Guidance literature:
Multi-step reaction with 3 steps
1: 92 percent / DABCO / CHCl3 / 72 h / Ambient temperature
2: 58 percent / 5 h / 100 °C
3: 32 percent / 1 h / 120 °C
With 1,4-diaza-bicyclo[2.2.2]octane; In chloroform;
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