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3-(9H-Carbazol-9-yl)phenylboronic acid

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CAS:864377-33-3
Purity:99%+HPLC Package:100g,500g,1kg,5kg,25kg
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CAS:864377-33-3
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CAS:864377-33-3
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Products Intro: Product Name:3-(9H-carbazol-9-yl)phenylboronic acid
CAS:864377-33-3
Purity:Not available Package:100g;1kg;5kg,10kg,25kg,50kg

3-(9H-Carbazol-9-yl)phenylboronic acid manufacturers

3-(9H-Carbazol-9-yl)phenylboronic acid Basic information
Product Name:3-(9H-Carbazol-9-yl)phenylboronic acid
Synonyms:3-(9H-Carbazol-9-yl)phenylboronic acid;3-(9H-carbazole-9-yl)phenylboronic acid;3-(9H-Carbazol-9-yl)phenylboromic acid;Boronic acid, [3-(9H-carbazol-9-yl)phenyl]-;3-(9-Carbazolyl)benzeneboronic acid, 98%;3-(9H-carbazol-9-yl)phenylboronic acid (3CPBA);Boronic acid,B-[3-(9H-carbazol-9-yl)phenyl]-;3-(9H-Carbazol-9-yl)phenylboronic Acid (contains varying amounts of Anhydride)
CAS:864377-33-3
MF:C18H14BNO2
MW:287.12
EINECS:
Product Categories:OLED materials,pharm chemical,electronic;OLED
Mol File:864377-33-3.mol
3-(9H-Carbazol-9-yl)phenylboronic acid Structure
3-(9H-Carbazol-9-yl)phenylboronic acid Chemical Properties
Boiling point 472.6±51.0 °C(Predicted)
density 1.20
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Powder
pka8.30±0.10(Predicted)
color Off-white
InChIInChI=1S/C18H14BNO2/c21-19(22)13-6-5-7-14(12-13)20-17-10-3-1-8-15(17)16-9-2-4-11-18(16)20/h1-12,21-22H
InChIKeyIDQUIFLAFFZYEX-UHFFFAOYSA-N
SMILESB(C1=CC=CC(N2C3=C(C=CC=C3)C3=C2C=CC=C3)=C1)(O)O
Safety Information
HS Code 2933998090
MSDS Information
3-(9H-Carbazol-9-yl)phenylboronic acid Usage And Synthesis
Chemical Propertiesoff-white solid
Usessuzuki reaction
Synthesis
9-(3-bromophenyl)carbazole

185112-61-2

Trimethyl borate

121-43-7

3-(9H-Carbazol-9-yl)phenylboronic acid

864377-33-3

General procedure for the synthesis of 3-(9H-carbazol-9-yl)phenylboronic acid from 9-(3-bromophenyl)-9H-carbazole and trimethyl borate: (2) Dissolve 4.00 g of 9-(3-bromophenyl)-9H-carbazole in dry 50 mL of THF, and cool to -78 °C. 6mL (2.4M) of n-butyllithium solution was slowly added and reacted for 1 hour. Subsequently, 1.8 mL of trimethyl borate was added and the reaction continued for 2 hours. The reaction mixture was warmed to room temperature and stirred overnight. After cooling to 0°C, 40 mL of 2.0 M HCl was added for hydrolysis. The reaction mixture was extracted with dichloromethane and the solvent was evaporated to give 2.96 g of 3-(9H-carbazol-9-yl)phenylboronic acid in 83% yield.

References[1] Patent: CN103588770, 2016, B. Location in patent: Paragraph 0047
[2] Patent: CN107686484, 2018, A. Location in patent: Paragraph 0129-0132
[3] Patent: WO2013/12298, 2013, A1. Location in patent: Paragraph 103-104
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