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1H-Isoindole-1,3(2H)-dione, 2-(3-phenylpropoxy)-

Base Information Edit
  • Chemical Name:1H-Isoindole-1,3(2H)-dione, 2-(3-phenylpropoxy)-
  • CAS No.:160725-45-1
  • Molecular Formula:C17H15NO3
  • Molecular Weight:281.311
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90438318
  • Wikidata:Q82254015
  • Mol file:160725-45-1.mol
1H-Isoindole-1,3(2H)-dione, 2-(3-phenylpropoxy)-

Synonyms:160725-45-1;1H-Isoindole-1,3(2H)-dione, 2-(3-phenylpropoxy)-;DTXSID90438318

Suppliers and Price of 1H-Isoindole-1,3(2H)-dione, 2-(3-phenylpropoxy)-
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 1H-Isoindole-1,3(2H)-dione, 2-(3-phenylpropoxy)- Edit
Chemical Property:
  • PSA:46.61000 
  • LogP:2.78490 
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:281.10519334
  • Heavy Atom Count:21
  • Complexity:366
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)CCCON2C(=O)C3=CC=CC=C3C2=O
Technology Process of 1H-Isoindole-1,3(2H)-dione, 2-(3-phenylpropoxy)-

There total 3 articles about 1H-Isoindole-1,3(2H)-dione, 2-(3-phenylpropoxy)- 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 di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20 ℃; Inert atmosphere;
DOI:10.1002/anie.201000160
Guidance literature:
With sodium hydride; In N,N-dimethyl-formamide; at 80 ℃; for 1h; Inert atmosphere;
DOI:10.1021/acs.joc.0c02557
Guidance literature:
Multi-step reaction with 2 steps
1: N,N`-sulfuryldiimidazole; potassium fluoride; tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine / trifluoroacetic acid; N,N-dimethyl-formamide / 0.17 h / 20 °C
2: sodium hydride / N,N-dimethyl-formamide / 1 h / 80 °C / Inert atmosphere
With potassium fluoride; tetra-(n-butyl)ammonium iodide; sodium hydride; N-ethyl-N,N-diisopropylamine; N,N`-sulfuryldiimidazole; In N,N-dimethyl-formamide; trifluoroacetic acid;
DOI:10.1021/acs.joc.0c02557
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