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Chemical Structure| 1189047-28-6 Chemical Structure| 1189047-28-6

Structure of 1189047-28-6

Chemical Structure| 1189047-28-6

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Product Details of [ 1189047-28-6 ]

CAS No. :1189047-28-6
Formula : C18H14BNO2
M.W : 287.12
SMILES Code : OB(C1=CC=CC=C1N2C3=C(C4=C2C=CC=C4)C=CC=C3)O
MDL No. :MFCD30543408
InChI Key :MBWDMWMXFNHYLL-UHFFFAOYSA-N
Pubchem ID :58121764

Safety of [ 1189047-28-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 1189047-28-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1189047-28-6 ]

[ 1189047-28-6 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 1189047-28-6 ]
  • [ 57103-20-5 ]
  • [ 1189047-29-7 ]
YieldReaction ConditionsOperation in experiment
With sodium carbonate;tetrakis(triphenylphosphine) palladium(0); In ethanol; water; toluene; at 80℃; for 15h; Example 5 Synthesis of Compound 11 In a 1,000-mL three-necked flask were placed 11.0 g (38.3 millimoles) of 2-carbazolylphenylboronic acid, 6.0 g (15.0 millimoles) of <strong>[57103-20-5]3,6-dibromo-9-phenylcarbazole</strong>, and 1.6 g (1.4 millimoles) of tetrakis(triphenylphosphine)palladium(0), then 100 mL of ethanol and 200 mL of toluene were added, and the mixture was stirred. Thereafter, a solution of 15.0 g (142.0 millimoles) of sodium carbonate in 200 mL of water was thrown into the flask. The mixture was then heated to 80°C and stirred for 15 hours. The reaction solution was cooled to room temperature, transferred to a 1,000-mL separatory funnel, and separated into an organic layer and an aqueous layer. The organic layer was washed three times with 200 mL of water and then dehydrated over magnesium sulfate, the magnesium sulfate was filtered off, and the solvent was distilled off under reduced pressure. The reaction mixture thus obtained was purified by recrystallization from THF and methanol to yield 5.1 g of Compound 11 as a white solid; EI-MS, 726 (M+1); melting point, 275°C; glass transition temperature, 143°C.
  • 2
  • [ 902518-11-0 ]
  • [ 11113-50-1 ]
  • [ 1189047-28-6 ]
  • 3
  • [ 121-43-7 ]
  • [ 902518-11-0 ]
  • [ 1189047-28-6 ]
YieldReaction ConditionsOperation in experiment
78% <strong>[902518-11-0]9-(2-bromophenyl)-9H-carbazole</strong> 4.00g of THF was added 50mL of dry, cooling to -78 deg.] C, n-butyllithium was slowly added 6mL (the 2.4M), for 1 hour, followed by after addition of trimethyl borate 1.8mL, reaction was continued for 2 hours. after the reaction warmed to room temperature overnight, cooled to 0 deg.] C, was added HCl (2.0 M) 40mL hydrolysis, and extracted with methylene chloride, the solvent was evaporated, to give 2.82g (2-(9H-carbazol-9-yl)phenyl)boronic acid in 78percent yield.
43% 9-(2-Bromophenyl)-9H-carbazole (1.6 g, 4.98 mmol) was dissolved in 40 mL of anhydrous THF solution and cooled to -78 °C. Then, 2 M n-BuLi (3.2 mL, 6.48 mmol) was dropped slowly. After stirring at -78 °C for 30 min, trimethylborate (2.22 mL, 20 mmol) was slowly added. The resulting mixture was stirred for 4 h and gradually warmed to room temperature. The reaction was quenched with water and extracted with ethyl acetate and water. The organic layer was dried with anhydrous MgSO4 and filtered. The solution was evaporated. Then, the residue was purified by recrystallized from hexane to give a white powder. (1.24 g, Yield 43percent) 1H NMR (300 MHz, DMSO): delta (ppm) 8.14-8.17 (d, 2H),7.85-7.88 (d, 1H), 7.47-7.57 (m, 2H), 7.37-7.45 (m, 3H), 7.27-7.32(m, 2H), 7.05-7.08 (d, 2H).
  • 4
  • [ 5419-55-6 ]
  • [ 902518-11-0 ]
  • [ 1189047-28-6 ]
YieldReaction ConditionsOperation in experiment
90% 9-(2-Bromophenyl)-9H-carbazole (1 eq), added to a dry tetrahydrofuran solution, cooled to -78 ° C, and exchanged N2 three times to ensure the system's oxygen-free environment.After adding n-butyllithium (2.5 M, 1.1 eq) dropwise, the reaction was kept at -78 ° C for 1.5 h.Triisopropyl borate (rho=0.815g/ml, 1.1eq) was added dropwise, and the mixture was added to room temperature after the addition was completed. After 8 hours, the reaction was quenched with dilute hydrochloric acid.The tetrahydrofuran was distilled off under reduced pressure, dissolved in dichloromethane, washed with water, anhydrous magnesium sulfate, dried, filtered, and the filtrate was recrystallized.Obtained a white solid product (90percent);
 

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