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1-Propanone, 3-(1-naphthalenyl)-1-phenyl-

Base Information
  • Chemical Name:1-Propanone, 3-(1-naphthalenyl)-1-phenyl-
  • CAS No.:96550-91-3
  • Molecular Formula:C19H16O
  • Molecular Weight:260.335
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80473617
  • Nikkaji Number:J1.531.326I
  • Wikidata:Q82303127
1-Propanone, 3-(1-naphthalenyl)-1-phenyl-

Synonyms:1-Propanone, 3-(1-naphthalenyl)-1-phenyl-;96550-91-3;SCHEMBL18662750;DTXSID80473617

Suppliers and Price of 1-Propanone, 3-(1-naphthalenyl)-1-phenyl-
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Chemical Property of 1-Propanone, 3-(1-naphthalenyl)-1-phenyl-
Chemical Property:
  • XLogP3:5.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:4
  • Exact Mass:260.120115130
  • Heavy Atom Count:20
  • Complexity:316
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C(=O)CCC2=CC=CC3=CC=CC=C32
Technology Process of 1-Propanone, 3-(1-naphthalenyl)-1-phenyl-

There total 14 articles about 1-Propanone, 3-(1-naphthalenyl)-1-phenyl- 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 phosphate; Wilkinson's catalyst; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In 1,4-dioxane; at 60 ℃; for 20h; under 750.075 Torr; Inert atmosphere;
DOI:10.1002/adsc.201200821
Guidance literature:
With C41H37ClN2P2Ru; caesium carbonate; In tert-Amyl alcohol; at 150 ℃; for 22h; Inert atmosphere; Green chemistry;
DOI:10.1002/chem.202000396
Guidance literature:
With diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; ephedrine; In toluene; at 60 ℃; for 48h; chemoselective reaction; Inert atmosphere;
DOI:10.14233/ajchem.2018.21480
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