1219956-23-6

  • Product Name2,4-Diphenyl-6-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine
  • Molecular FormulaC27H26BN3O2
  • Molecular Weight435.3
  • Purity99%
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Product Details

Quick Details

  • CasNo: 1219956-23-6
  • Molecular Formula: C27H26BN3O2
  • Purity: 99%

Factory Supply High Quality 1219956-23-6 2,4-Diphenyl-6-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine

  • Molecular Formula:C27H26BN3O2
  • Molecular Weight:435.32524
  • Melting Point:210.0 to 214.0 °C 
  • Boiling Point:625.6±57.0 °C(Predicted) 
  • PKA:0.66±0.10(Predicted) 
  • PSA:57.13000 
  • Density:1.21±0.1 g/cm3(Predicted) 
  • LogP:5.17180 

2,4-Diphenyl-6-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine(Cas 1219956-23-6) Usage

Purity and Storage Purity: Minimum 98% (GC)
Storage Temperature: Ambient
Chemical Structure Comprises 2,4-Diphenyl-6-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine.
Functional Groups Contains phenyl rings, a triazine ring, and a reactive boronic acid group. Boronic acid groups are known for their reactivity in certain chemical reactions, such as Suzuki-Miyaura coupling.
Uses Compounds with boronic acid functionalities are commonly used in organic synthesis, especially in Suzuki-Miyaura coupling reactions. These reactions are instrumental in constructing biaryl compounds.

InChI:InChI=1/C10H9BO2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7,12-13H

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Mix 2-(2-bromophenyl)-9-phenyl-9H-carbazole (1 g, 2.51 mmol), 2,4-diphenyl-6-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,3,5-triazine (1.2 g, 2.76 mmol), K2CO3 (0.7 g, 5.06 mmol) and Pd(PPh3)2Cl2 (0.02 g, 0.03 mmol) in a three-necked flask, followed by toluene (10 mL), ethanol (5 mL) and deionized water (5 mL).

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1219956-23-6 Process route

1.4-dibromobenzene
106-37-6

1.4-dibromobenzene

2,4-diphenyl-6-(4-(4<SUB>,</SUB>4<SUB>',</SUB>5,5'-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,3,5-triazine
1219956-23-6

2,4-diphenyl-6-(4-(4,4',5,5'-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,3,5-triazine

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1: potassium acetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 12 h / 100 °C
2: potassium carbonate; tetrakis(triphenylphosphine) palladium(0) / tetrahydrofuran; water / 12 h / 120 °C
3: potassium acetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 12 h / 100 °C
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tetrakis(triphenylphosphine) palladium(0); potassium acetate; potassium carbonate; In tetrahydrofuran; 1,4-dioxane; water;
 
p-bromophenylboronic acid pinacol ester
68716-49-4

p-bromophenylboronic acid pinacol ester

2,4-diphenyl-6-(4-(4<SUB>,</SUB>4<SUB>',</SUB>5,5'-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,3,5-triazine
1219956-23-6

2,4-diphenyl-6-(4-(4,4',5,5'-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,3,5-triazine

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: potassium carbonate; tetrakis(triphenylphosphine) palladium(0) / tetrahydrofuran; water / 12 h / 120 °C
2: potassium acetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 12 h / 100 °C
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tetrakis(triphenylphosphine) palladium(0); potassium acetate; potassium carbonate; In tetrahydrofuran; 1,4-dioxane; water;
 

1219956-23-6 Upstream products

  • 106-37-6
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  • 68716-49-4
    68716-49-4

    p-bromophenylboronic acid pinacol ester

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