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1,4-Diphenyl-5,5-dimethyl-1,3-cyclopentadiene

Base Information
  • Chemical Name:1,4-Diphenyl-5,5-dimethyl-1,3-cyclopentadiene
  • CAS No.:33930-83-5
  • Molecular Formula:C19H18
  • Molecular Weight:246.352
  • Hs Code.:
  • DSSTox Substance ID:DTXSID101184161
  • Nikkaji Number:J3.242.808H
1,4-Diphenyl-5,5-dimethyl-1,3-cyclopentadiene

Synonyms:DTXSID101184161;AKOS024321604;1,4-Diphenyl-5,5-dimethyl-1,3-cyclopentadiene;(5,5-dimethyl-4-phenyl-1,3-cyclopentadien-1-yl)benzene;1,1'-(2,2-Dimethyl-3,5-cyclopentadiene-1,3-diyl)bis[benzene];33930-83-5

Suppliers and Price of 1,4-Diphenyl-5,5-dimethyl-1,3-cyclopentadiene
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 1,4-Diphenyl-5,5-dimethyl-1,3-cyclopentadiene
Chemical Property:
  • XLogP3:5.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:2
  • Exact Mass:246.140850574
  • Heavy Atom Count:19
  • Complexity:335
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1(C(=CC=C1C2=CC=CC=C2)C3=CC=CC=C3)C
Technology Process of 1,4-Diphenyl-5,5-dimethyl-1,3-cyclopentadiene

There total 7 articles about 1,4-Diphenyl-5,5-dimethyl-1,3-cyclopentadiene 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 potassium fluoride; tris-(dibenzylideneacetone)dipalladium(0); tricyclohexylphosphine; In tetrahydrofuran; water; at 20 ℃; for 12h; Inert atmosphere; Schlenk technique;
DOI:10.1021/ol402824m
Guidance literature:
Multi-step reaction with 2 steps
1: potassium hexamethylsilazane / tetrahydrofuran / 5 h / -78 °C / Inert atmosphere
2: potassium fluoride; tris-(dibenzylideneacetone)dipalladium(0); tricyclohexylphosphine / tetrahydrofuran; water / 12 h / 20 °C / Inert atmosphere; Schlenk technique
With potassium fluoride; tris-(dibenzylideneacetone)dipalladium(0); potassium hexamethylsilazane; tricyclohexylphosphine; In tetrahydrofuran; water;
DOI:10.1021/ol402824m
Guidance literature:
Multi-step reaction with 2 steps
1: potassium bromide; potassium phenolate; bis-triphenylphosphine-palladium(II) chloride; triphenylphosphine / toluene / 12 h / 60 °C / Inert atmosphere; Schlenk technique
2: tetrabutylammomium bromide; potassium carbonate; tetrakis(triphenylphosphine) palladium(0) / water; ethanol / 72 h / 100 °C / Inert atmosphere; Schlenk technique
With bis-triphenylphosphine-palladium(II) chloride; tetrakis(triphenylphosphine) palladium(0); potassium phenolate; tetrabutylammomium bromide; potassium carbonate; triphenylphosphine; potassium bromide; In ethanol; water; toluene;
DOI:10.1021/ol402824m
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