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2-Phenylindan

Base Information
  • Chemical Name:2-Phenylindan
  • CAS No.:22253-11-8
  • Molecular Formula:C15H14
  • Molecular Weight:194.276
  • Hs Code.:2902909090
  • European Community (EC) Number:244-872-2
  • UNII:YT55G9EFN6
  • DSSTox Substance ID:DTXSID00176794
  • Nikkaji Number:J285.467H
  • Wikidata:Q83047090
  • Mol file:22253-11-8.mol
2-Phenylindan

Synonyms:2-Phenylindan;2,3-dihydro-2-phenyl-1H-indene;22253-11-8;1H-Indene, 2,3-dihydro-2-phenyl-;YT55G9EFN6;EINECS 244-872-2;UNII-YT55G9EFN6;INDAN, 2-PHENYL-;DTXSID00176794;AKOS006317422

Suppliers and Price of 2-Phenylindan
Supply Marketing:
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
  • American Custom Chemicals Corporation
  • 2-PHENYLINDAN 95.00%
  • 5MG
  • $ 500.31
Total 5 raw suppliers
Chemical Property of 2-Phenylindan
Chemical Property:
  • Vapor Pressure:0.00751mmHg at 25°C 
  • Refractive Index:1.5955 
  • Boiling Point:277.7°Cat760mmHg 
  • Flash Point:120.8°C 
  • PSA:0.00000 
  • Density:1.063g/cm3 
  • LogP:3.56900 
  • XLogP3:4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:1
  • Exact Mass:194.109550447
  • Heavy Atom Count:15
  • Complexity:188
Purity/Quality:

98%Min *data from raw suppliers

2-PHENYLINDAN 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C(CC2=CC=CC=C21)C3=CC=CC=C3
Technology Process of 2-Phenylindan

There total 33 articles about 2-Phenylindan 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 mercury(II) oxide; In ethanol; at 62 ℃; for 4.25h;
Guidance literature:
With [4,4′-bis(1,1-dimethylethyl)-2,2′-bipyridine-N1,N1′]bis{3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC}iridium(III) hexafluorophosphate; methylamine hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 25 ℃; Irradiation;
DOI:10.1002/anie.201905485
Guidance literature:
With N-ethyl-N,N-diisopropylamine; triphenylphosphine; 4,4'-di-tert-butyl-2,2'-bipyridine; lithium bromide; nickel dibromide; In 1-methyl-pyrrolidin-2-one; at 20 ℃; for 14h; Glovebox; Electrolysis;
DOI:10.1021/jacs.0c13093
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