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| | 2,4-Diphenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine Basic information |
| Product Name: | 2,4-Diphenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine | | Synonyms: | 2,4-Diphenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine;2-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-4,6-diphenyl-1,3,5-triazine;2,4-Diphenyl-6-(3-boronate)-1,3,5-triazine;1,3,5-Triazine, 2,4-diphenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-;2-[3-(4,6-Diphenyl-1,3,5-triazin-2-yl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;3-(4,6-Diphenyl-1,3,5-triazine-2-yl)phenylboronic Acid Pinacol Ester;2-dioxaborolan-2-yl)phenyl]-1;4-Diphenyl-6-[3-(4 | | CAS: | 1269508-31-7 | | MF: | C27H26BN3O2 | | MW: | 435.33 | | EINECS: | | | Product Categories: | | | Mol File: | 1269508-31-7.mol | ![2,4-Diphenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine Structure](CAS/20150408/GIF/1269508-31-7.gif) |
| | 2,4-Diphenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine Chemical Properties |
| Melting point | 204 °C | | Boiling point | 641.3±57.0 °C(Predicted) | | density | 1.21±0.1 g/cm3(Predicted) | | form | powder to crystal | | pka | 0.92±0.10(Predicted) | | color | White to Almost white |
| | 2,4-Diphenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine Usage And Synthesis |
| Uses | 2,4-Diphenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine can be used as an intermediate in organic
synthesis, mainly used in laboratory research and development and
chemical production processes. | | Synthesis | 
15.0 g of 2-(3-Bromophenyl)-4,6-diphenyl-l,3,5-
triazine (32.4 mmol), 12.3 g of bis(pinacolato)diboron (48.6
mmol), 529 mg of Pd(dppf)Cl2.CH2Cl2 (0.647 mmol), 9.53
g of potassium acetate (97.1 mmol) and 323 ml of dioxane
were put into a 1-neck round flask and reacted under reflux
at 90° C. for 12 hours. After completion of the reaction, the solvent was removed under reduced pressure. The produced
solid was dissolved in dichloromethane and then filtered
through a Celite filter and washed with dichloromethane.
The solvent was removed under reduced pressure and the
resultant compound was crystallized with methanol to obtain
16.0 g of solid compound (intermediate 6) (yield: 96.8%). |
| | 2,4-Diphenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine Preparation Products And Raw materials |
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