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Encyclopedia

o-Quaterphenyl

Base Information Edit
  • Chemical Name:o-Quaterphenyl
  • CAS No.:641-96-3
  • Molecular Formula:C24H18
  • Molecular Weight:306.407
  • Hs Code.:2916399090
  • Mol file:641-96-3.mol
o-Quaterphenyl

Synonyms:Biphenyl,2,2'-diphenyl- (4CI,6CI); o-Quaterphenyl (7CI,8CI); 1,1'-Biphenyl,2,2'-diphenyl-; 2,2'-Diphenylbiphenyl; NSC 90717; o,o-Quaterphenyl;o,o'-Quaterphenyl

Suppliers and Price of o-Quaterphenyl
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
  • TRC
  • 1,1'':2'',1'''':2'''',1''''''-Quaterphenyl
  • 250mg
  • $ 165.00
  • Medical Isotopes, Inc.
  • 1,1??:2??,1????:2????,1??????-Quaterphenyl
  • 2.5 g
  • $ 2200.00
Total 4 raw suppliers
Chemical Property of o-Quaterphenyl Edit
Chemical Property:
  • Melting Point:118.5°C 
  • Refractive Index:1.9130 (estimate) 
  • Boiling Point:382.01°C (rough estimate) 
  • Flash Point:201.2oC 
  • PSA:0.00000 
  • Density:1.1138 (estimate) 
  • LogP:6.68760 
Purity/Quality:

99% *data from raw suppliers

1,1'':2'',1'''':2'''',1''''''-Quaterphenyl *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 1,1'':2'',1'''':2'''',1''''''-Quaterphenyl is a catalyst for electrochemical reduction of the alkyl chlorides. It is also an intermediate used to prepare Dibenzo[e,l]pyrene (D417375) which is possibly carcinogenic.
Technology Process of o-Quaterphenyl

There total 83 articles about o-Quaterphenyl 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 bis(acetylacetonate)nickel(II); In diethyl ether; benzene; 1.) 0 deg C, 1 h, 2.) reflux, 3 h;
DOI:10.1246/bcsj.53.821
Guidance literature:
With bis(acetylacetonate)nickel(II); In benzene; 1) 0 deg C, 1h; 2) reflux, 3 h;
Guidance literature:
2-Bromobiphenyl; methylzinc chloride; With n-butyllithium; In tetrahydrofuran; diethyl ether; hexane; at 0 ℃; for 0.5h;
With oxovanadium(V) ethoxydichloride; In tetrahydrofuran; diethyl ether; hexane; at 20 ℃; for 10h; Further stages.;
DOI:10.1021/jo9919106
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