p-Terphenyl, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-

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p-Terphenyl, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)- Basic information
Product Name:p-Terphenyl, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-
Synonyms:p-Terphenyl, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-;[1,1':4',1''-Terphenyl]-4-boronic acid pinacol ester;4,4,5,5-Tetramethyl-2-[1,1':4',1''-terphenyl]-4-yl-1,3,2-dioxaborolane;2-([1,1':4',1''-Terphenyl]-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;2-([1,1':4',1''-Terphenyl]-4-yl);2-([1,1':4',1"-terphenyl]-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxabolorane;1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[1,1':4',1''-terphenyl]-4-yl-;(1,1':4',1''-Terphenyl)-4-ylboronic Acid Pinacol Ester
CAS:1080632-76-3
MF:C24H25BO2
MW:356.27
EINECS:
Product Categories:OLED
Mol File:1080632-76-3.mol
p-Terphenyl, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)- Structure
p-Terphenyl, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)- Chemical Properties
Melting point 146 °C
Boiling point 508.5±29.0 °C(Predicted)
density 1.10
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
AppearanceWhite to off-white Solid
Safety Information
HS Code 2931.90.6000
MSDS Information
p-Terphenyl, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)- Usage And Synthesis
Synthesis
4-BROMO-P-TERPHENYL

1762-84-1

Bis(pinacolato)diboron

73183-34-3

p-Terphenyl, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-

1080632-76-3

General procedure for the synthesis of [1,1':4',1''-terphenyl]-4-boronic acid pinacol ester from 4-bromo-p-terphenyl and bis(pinacolato)diboronic acid: 4-bromo-p-terphenyl (120 g, 388 mmol) was dissolved in 1.2 L of dimethylformamide (DMF) under nitrogen protection. Subsequently, bis(pinacolato)diboron (118 g, 466 mmol), 1,1'-bis(diphenylphosphino)ferric-palladium(II) dichloride (3.17 g, 3.88 mmol) and potassium acetate (114 g, 1,164 mmol) were added. The reaction mixture was heated to reflux at 150 °C for 4 hours. After completion of the reaction, the reaction solution was poured into water and the precipitate was collected by filtration. The resulting solid was dried in a vacuum oven. Finally, the crude product was separated and purified by fast column chromatography to afford [1,1':4',1''-terphenyl]-4-boronic acid pinacol ester (124 g, 90% yield).

References[1] Patent: KR2015/117173, 2015, A. Location in patent: Paragraph 0284-0286
[2] Patent: US2017/331067, 2017, A1. Location in patent: Paragraph 0248-0251
[3] Patent: US2017/40550, 2017, A1. Location in patent: Paragraph 0083
p-Terphenyl, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)- Preparation Products And Raw materials
Raw materials4-Bromo-p-terphenyl-->Bis(pinacolato)diboron-->Potassium Acetate-->N,N-Dimethylformamide
Tag:p-Terphenyl, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-(1080632-76-3) Related Product Information
p-Terphenyl-d14 Benzene,(trans-4-propylcyclohexyl)- 4-Biphenylboronic acid, pinacol ester 4,4'-Biphenyldiboronic acid dipinacol ester 4,4,5,5-TetraMethyl-2-[4-(4-Methylphenyl)phenyl]-1,3,2-dioxaborolane 2-[4-[3,5-bis[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]phenyl]phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane