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Boronic acid, [4-fluoro-3-(3-fluoro-2-pyridinyl)phenyl]-

Base Information Edit
  • Chemical Name:Boronic acid, [4-fluoro-3-(3-fluoro-2-pyridinyl)phenyl]-
  • CAS No.:425379-45-9
  • Molecular Formula:C11H8BF2NO2
  • Molecular Weight:234.998
  • Hs Code.:
  • Mol file:425379-45-9.mol
Boronic acid, [4-fluoro-3-(3-fluoro-2-pyridinyl)phenyl]-

Synonyms:

Suppliers and Price of Boronic acid, [4-fluoro-3-(3-fluoro-2-pyridinyl)phenyl]-
Supply Marketing:Edit
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Boronic acid, [4-fluoro-3-(3-fluoro-2-pyridinyl)phenyl]- Edit
Chemical Property:
Purity/Quality:

95%-98% *data from raw suppliers

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Technology Process of Boronic acid, [4-fluoro-3-(3-fluoro-2-pyridinyl)phenyl]-

There total 4 articles about Boronic acid, [4-fluoro-3-(3-fluoro-2-pyridinyl)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:
2-(5-bromo-2-fluorophenyl)-3-fluoropyridine; With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-5,5-dimethyl-1,3,2-dioxaborinane; In 1,4-dioxane; dichloromethane; at 80 ℃; for 18h;
With hydrogenchloride; at 45 ℃; for 0.5h;
DOI:10.1021/jm051144x
Guidance literature:
Multi-step reaction with 2 steps
1.1: 69 percent / dibromodimethylhydantoin; sulfuric acid / acetonitrile / 2 h / 55 °C
2.1: bis(neopentylglycolato)diboron; potassium acetate; dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) / dioxane; CH2Cl2 / 18 h / 80 °C
2.2: 94 percent / aq. HCl / 0.5 h / 45 °C
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; sulfuric acid; potassium acetate; 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-5,5-dimethyl-1,3,2-dioxaborinane; In 1,4-dioxane; dichloromethane; acetonitrile;
DOI:10.1021/jm051144x
Guidance literature:
Multi-step reaction with 3 steps
1.1: 86 percent / potassium fluoride; tris(dibenzylideneacetone)dipalladium (0); tri-tert-butylphosphine / tetrahydrofuran; H2O; hexane / 24 h / 55 °C
2.1: 69 percent / dibromodimethylhydantoin; sulfuric acid / acetonitrile / 2 h / 55 °C
3.1: bis(neopentylglycolato)diboron; potassium acetate; dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) / dioxane; CH2Cl2 / 18 h / 80 °C
3.2: 94 percent / aq. HCl / 0.5 h / 45 °C
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium fluoride; tris(dibenzylideneacetone)dipalladium (0); 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; tri-tert-butyl phosphine; sulfuric acid; potassium acetate; 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-5,5-dimethyl-1,3,2-dioxaborinane; In tetrahydrofuran; 1,4-dioxane; hexane; dichloromethane; water; acetonitrile; 1.1: Suzuki coupling;
DOI:10.1021/jm051144x
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