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4-(9H-Carbozol-9-yl)phenylboronic acid

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4-(9H-Carbozol-9-yl)phenylboronic acid Basic information

Product Name:
4-(9H-Carbozol-9-yl)phenylboronic acid
Synonyms:
  • BORONIC ACID, [4-(9H-CARBAZOL-9-YL)PHENYL]-
  • 4-(9-Carbazolyl)benzeneboronic acid, 98%
  • 4-(9-Carbazolyl)phenylboronic Acid
  • 4-(Carbazole-9-Yl)Phenyl Boronic Acid
  • B-[4-(9H-carbazol-9-yl)phenyl]- Boronic acid
  • 4-(9H-carbazole-9-yl)phenylboronic acid (4CPBA)
  • 3-(9H-9-carbazol-9-yl)phenylboronic acid
  • NBAPC
CAS:
419536-33-7
MF:
C18H14BNO2
MW:
287.12
EINECS:
808-009-9
Product Categories:
  • OLED materials,pharm chemical,electronic
Mol File:
419536-33-7.mol
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4-(9H-Carbozol-9-yl)phenylboronic acid Chemical Properties

Melting point:
264°C(lit.)
Boiling point:
452.7±51.0 °C(Predicted)
Density 
1.20±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
Powder
pka
8.14±0.17(Predicted)
color 
Off-white
InChI
InChI=1S/C18H14BNO2/c21-19(22)13-9-11-14(12-10-13)20-17-7-3-1-5-15(17)16-6-2-4-8-18(16)20/h1-12,21-22H
InChIKey
JGAVTCVHDMOQTJ-UHFFFAOYSA-N
SMILES
B(C1=CC=C(N2C3=C(C=CC=C3)C3=C2C=CC=C3)C=C1)(O)O
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Safety Information

HS Code 
29339900
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4-(9H-Carbozol-9-yl)phenylboronic acid Usage And Synthesis

Chemical Properties

Class white powder

Uses

suzuki reaction

Synthesis

57102-42-8

419536-33-7

General procedure for the synthesis of 4-(9-carbazolyl)phenylboronic acid from 9-(4-bromophenyl)carbazole: 9-(4-bromophenyl)carbazole (35 g, 108.6 mmol) was dissolved in tetrahydrofuran (THF, 600 mL), and n-butyllithium (n-BuLi, 52 mL, 130.35 mmol, -78 °C) was slowly added to the reaction system. 2.5 M hexane solution). The reaction mixture was stirred at this temperature for 1 hour. Subsequently, the reaction system was slowly warmed to room temperature and triisopropoxyborane (B(Oi-Pr)3, 37 mL, 162.9 mmol) was added dropwise to the reaction mixture during this process. The reaction mixture was continued to be stirred at room temperature for 12 hours. Upon completion of the reaction, extraction was carried out with ethyl acetate (EA), the organic layers were combined and dried over anhydrous magnesium sulfate (MgSO4) to remove water. Subsequently, the solvent was removed by distillation under reduced pressure and the crude product obtained was recrystallized by a solvent mixture of ethyl acetate and hexane to give 4-(9-carbazolyl)phenylboronic acid (25 g, 81% yield).

References

[1] Organic and Biomolecular Chemistry, 2012, vol. 10, # 33, p. 6693 - 6704
[2] Australian Journal of Chemistry, 2007, vol. 60, # 8, p. 603 - 607
[3] Physical Chemistry Chemical Physics, 2011, vol. 13, # 39, p. 17825 - 17830
[4] Organic and Biomolecular Chemistry, 2012, vol. 10, # 47, p. 9481 - 9490
[5] Patent: WO2013/12297, 2013, A1. Location in patent: Paragraph 111; 114; 115

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