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Phosphine oxide, (2-methoxyphenyl)diphenyl-

Base Information
  • Chemical Name:Phosphine oxide, (2-methoxyphenyl)diphenyl-
  • CAS No.:51986-54-0
  • Molecular Formula:C19H17O2P
  • Molecular Weight:308.317
  • Hs Code.:
  • European Community (EC) Number:807-450-4
  • DSSTox Substance ID:DTXSID90385196
  • Nikkaji Number:J488.521J
  • Wikidata:Q82177830
  • ChEMBL ID:CHEMBL1567278
  • Mol file:51986-54-0.mol
Phosphine oxide, (2-methoxyphenyl)diphenyl-

Synonyms:51986-54-0;Phosphine oxide, (2-methoxyphenyl)diphenyl-;(2-methoxyphenyl)diphenylphosphine oxide;(2-methoxyphenyl)(diphenyl)phosphane oxide;1-diphenylphosphoryl-2-methoxybenzene;CBMicro_012410;HMS2829J08;o-diphenylphosphinylanisole;MLS001008559;CHEMBL1567278;SCHEMBL14259711;Diphenyl(o-anisyl)phosphine oxide;DTXSID90385196;SMSF0003443;STK214175;(2-methoxyphenyl)diphenylphosphineoxide;AKOS003664426;CB15629;SMR000495808;(2-Methoxy-phenyl)diphenyl-phosphine oxide;(2-methoxyphenyl)(diphenyl)phosphine oxide;BIM-0012256.P001;phosphorane, (2-methoxyphenyl)diphenyl-, oxide;J-500838

Suppliers and Price of Phosphine oxide, (2-methoxyphenyl)diphenyl-
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
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Total 2 raw suppliers
Chemical Property of Phosphine oxide, (2-methoxyphenyl)diphenyl-
Chemical Property:
  • PSA:36.11000 
  • LogP:3.33460 
  • XLogP3:4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:308.09661678
  • Heavy Atom Count:22
  • Complexity:361
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=CC=CC=C1P(=O)(C2=CC=CC=C2)C3=CC=CC=C3
Technology Process of Phosphine oxide, (2-methoxyphenyl)diphenyl-

There total 14 articles about Phosphine oxide, (2-methoxyphenyl)diphenyl- 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 copper(l) iodide; (S)-1-phenyl-ethylamine; potassium carbonate; In toluene; at 110 ℃; for 24h; Inert atmosphere;
DOI:10.1016/j.tet.2012.10.064
Guidance literature:
With dihydrogen peroxide; In dichloromethane; at 0 - 20 ℃; for 1h;
Guidance literature:
With (1,2-dimethoxyethane)dichloronickel(II); titanium(IV) oxide; caesium carbonate; 4,4'-di-tert-butyl-2,2'-bipyridine; In acetonitrile; at 20 ℃; for 24h; Sealed tube; Sonication; Inert atmosphere; Irradiation;
DOI:10.1039/d0dt03507f
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