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2-(2-Phenylethyl)chromone

Base Information Edit
  • Chemical Name:2-(2-Phenylethyl)chromone
  • CAS No.:61828-53-3
  • Molecular Formula:C17H14 O2
  • Molecular Weight:250.297
  • Hs Code.:2914190090
  • DSSTox Substance ID:DTXSID90210818
  • Nikkaji Number:J19.454I
  • Wikidata:Q27106650
  • Metabolomics Workbench ID:69050
  • ChEMBL ID:CHEMBL481060
  • Mol file:61828-53-3.mol
2-(2-Phenylethyl)chromone

Synonyms:2-(2-phenylethyl)chromone

Suppliers and Price of 2-(2-Phenylethyl)chromone
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
  • Arctom
  • 2-(2-Phenylethyl)chromone ≥98%
  • 20mg
  • $ 188.00
Total 7 raw suppliers
Chemical Property of 2-(2-Phenylethyl)chromone Edit
Chemical Property:
  • Vapor Pressure:2.18E-06mmHg at 25°C 
  • Melting Point:90-91 °C(Solv: ligroine (8032-32-4); ethyl ether (60-29-7)) 
  • Boiling Point:393.1°C at 760 mmHg 
  • Flash Point:176.3°C 
  • PSA:30.21000 
  • Density:1.173g/cm3 
  • LogP:3.57820 
  • XLogP3:4.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:250.099379685
  • Heavy Atom Count:19
  • Complexity:352
Purity/Quality:

99%min. *data from raw suppliers

2-(2-Phenylethyl)chromone ≥98% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)CCC2=CC(=O)C3=CC=CC=C3O2
Technology Process of 2-(2-Phenylethyl)chromone

There total 9 articles about 2-(2-Phenylethyl)chromone 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:
o-hydroxyacetophenone; 3-phenylpropanoate; With sodium hydride; In tetrahydrofuran; mineral oil; for 0.0833333h; Reflux; Inert atmosphere;
With hydrogenchloride; In methanol; water; at 20 ℃; for 14h; Inert atmosphere;
DOI:10.1039/c8cc07787h
Guidance literature:
With chlorocarbonylbis(triphenylphosphine)rhodium(I); potassium carbonate; In N,N-dimethyl acetamide; at 90 ℃; for 5h; Schlenk technique; Inert atmosphere;
DOI:10.1039/c9ob02670c
Guidance literature:
With hydrogenchloride; acetic acid; In water; Reflux;
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