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618442-57-2

618442-57-2 Structure

618442-57-2 Structure
IdentificationBack Directory
[Name]

9-Phenyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
[CAS]

618442-57-2
[Synonyms]

3,6-Bis(4,4,5,5-tetramethyl-1,3,2
9-Phenyl-3,6-bis(4,4,5,5- tetraMethyl-1,3,2-dioxaborol
9-Phenyl-9H-carbazole-3,6-diboronic Acid Bis(pinacol) Ester
9-Phenyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)carbazole
3,6-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9-phenylcarbazole
9-Phenyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
9-Phenyl-3,6-bis(4,4,5,5- tetraMethyl-1,3,2-dioxaborolan- 2-yl)-9H-carbazol
3,6-Bis(4,4,5,5-tetramethyl-1,3,2- dioxaborolan-2-yl)-9-phenyl-9H-carbazole
9H-Carbazole, 9-phenyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
[Molecular Formula]

C30H35B2NO4
[MDL Number]

MFCD28015750
[MOL File]

618442-57-2.mol
[Molecular Weight]

495.225
Chemical PropertiesBack Directory
[Melting point ]

238.0 to 242.0 °C
[Boiling point ]

587.8±43.0 °C(Predicted)
[density ]

1.11±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

powder to crystal
[color ]

White to Light yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2934.99.4400
Spectrum DetailBack Directory
[Spectrum Detail]

9-Phenyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(618442-57-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Bis(pinacolato)diboron

73183-34-3

3,6-Dibromo-9-phenyl-9H-carbazole

57103-20-5

9-Phenyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole

618442-57-2

3,6-Dibromo-9-phenylcarbazole (0.075 mol) and pinacol ester of bisboronic acid (0.164 mol) were dissolved in 300 mL of dioxane and potassium acetate (0.375 mol) and tetrakis(triphenylphosphine)palladium (0.00075 mol) were added sequentially. The reaction mixture was heated to reflux for 5 hours. Upon completion of the reaction, the reaction was quenched with dichloromethane and water. The organic phase was separated and filtered through a silica gel funnel. Subsequently, the organic phase was concentrated under reduced pressure to remove the solvent. Finally, the resulting solid was purified by column chromatography to afford the target product 9-phenyl-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole (45% yield).

[References]

[1] Patent: CN106928237, 2017, A. Location in patent: Paragraph 0212; 0213; 0214
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