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1-(2-nitrophenyl)-1H-indole

Base Information
  • Chemical Name:1-(2-nitrophenyl)-1H-indole
  • CAS No.:25688-25-9
  • Molecular Formula:C14H10N2O2
  • Molecular Weight:238.246
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40436046
  • Nikkaji Number:J2.449.386E
  • Wikidata:Q82251233
  • ChEMBL ID:CHEMBL210554
  • Mol file:25688-25-9.mol
1-(2-nitrophenyl)-1H-indole

Synonyms:1-(2-nitrophenyl)-1H-indole;25688-25-9;1-(2-nitrophenyl)indole;N-(2-nitrophenyl) Indole;CHEMBL210554;SCHEMBL5661381;DTXSID40436046;FEYPDHWHOMTKCV-UHFFFAOYSA-N;STK689723

Suppliers and Price of 1-(2-nitrophenyl)-1H-indole
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
Total 6 raw suppliers
Chemical Property of 1-(2-nitrophenyl)-1H-indole
Chemical Property:
  • XLogP3:3.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:238.074227566
  • Heavy Atom Count:18
  • Complexity:315
Purity/Quality:

95% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C=CN2C3=CC=CC=C3[N+](=O)[O-]
Technology Process of 1-(2-nitrophenyl)-1H-indole

There total 11 articles about 1-(2-nitrophenyl)-1H-indole 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 sodium hydroxide; In dimethyl sulfoxide;
DOI:10.1039/d0ra06871c
Guidance literature:
1-(p-toluenesulfonyl)-1H-indole; With potassium tert-butylate; In tetrahydrofuran; for 1h; Inert atmosphere; Reflux;
ortho-nitrofluorobenzene; In tetrahydrofuran; for 3h; Reflux; Inert atmosphere;
DOI:10.1248/cpb.57.321
Guidance literature:
With tris(dibenzylideneacetone)dipalladium(0) chloroform complex; tri-tert-butyl phosphine; sodium t-butanolate; In toluene; at 90 ℃; for 12h;
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