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10-(4-Chlorophenyl)phenanthren-9-OL

Base Information
  • Chemical Name:10-(4-Chlorophenyl)phenanthren-9-OL
  • CAS No.:110210-89-4
  • Molecular Formula:C20H13ClO
  • Molecular Weight:304.776
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40549125
  • Wikidata:Q82428044
10-(4-Chlorophenyl)phenanthren-9-OL

Synonyms:110210-89-4;10-(4-CHLOROPHENYL)PHENANTHREN-9-OL;DTXSID40549125

Suppliers and Price of 10-(4-Chlorophenyl)phenanthren-9-OL
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 10-(4-Chlorophenyl)phenanthren-9-OL
Chemical Property:
  • XLogP3:6.3
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:304.0654927
  • Heavy Atom Count:22
  • Complexity:376
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C3=CC=CC=C3C(=C2C4=CC=C(C=C4)Cl)O
Technology Process of 10-(4-Chlorophenyl)phenanthren-9-OL

There total 4 articles about 10-(4-Chlorophenyl)phenanthren-9-OL 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 isopropylmagnesium bromide; bis(acetylacetonate)nickel(II); In diethyl ether; benzene; at -15 ℃; for 2h;
DOI:10.1016/S0040-4039(00)85196-5
Guidance literature:
With sodium methylate; In toluene; at 70 ℃; for 0.5h; regioselective reaction; Inert atmosphere;
DOI:10.1002/anie.201209269
Guidance literature:
Multi-step reaction with 3 steps
1: tris-(dibenzylideneacetone)dipalladium(0); tri tert-butylphosphoniumtetrafluoroborate; potassium fluoride dihydrate / tetrahydrofuran / 12 h / 40 °C / Inert atmosphere
2: toluene / 0.5 h / 70 °C / Inert atmosphere; Schlenk technique
3: sodium methylate / toluene / 0.5 h / 70 °C / Inert atmosphere
With tris-(dibenzylideneacetone)dipalladium(0); potassium fluoride dihydrate; sodium methylate; tri tert-butylphosphoniumtetrafluoroborate; In tetrahydrofuran; toluene; 1: |Suzuki-Miyaura Coupling;
DOI:10.1002/anie.201209269
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