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864377-33-3

864377-33-3 Structure

864377-33-3 Structure
IdentificationBack Directory
[Name]

3-(9H-Carbazol-9-yl)phenylboronic acid
[CAS]

864377-33-3
[Synonyms]

-9-yL
3-NBAPC
(3-(9H-CarbazoL
3-(9-Carbazolyl)benzeneboronicacid,98%
3-(9H-Carbazol-9-yl)phenylboronic acid
3-(9H-Carbazol-9-yl)phenylboromic acid
3-(9H-carbazole-9-yl)phenylboronic acid
3-(9H-Carbazol-9-yl)benzeneboronic Acid
3-(9-Carbazolyl)benzeneboronic acid, 98%
Boronic acid, [3-(9H-carbazol-9-yl)phenyl]-
Boronic acid,B-[3-(9H-carbazol-9-yl)phenyl]-
3-(9 H- carbazole-9-based phenylboronic acid
3-(9H-carbazol-9-yl)phenylboronic acid (3CPBA)
3-(9H-Carbazol-9-yl)phenylboronic acid ISO 9001:2015 REACH
3-(9H-Carbazol-9-yl)phenylboronic Acid (contains varying amounts of Anhydride)
[Molecular Formula]

C18H14BNO2
[MDL Number]

MFCD18072506
[MOL File]

864377-33-3.mol
[Molecular Weight]

287
Chemical PropertiesBack Directory
[Boiling point ]

472.6±51.0 °C(Predicted)
[density ]

1.20
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

Powder
[pka]

8.30±0.10(Predicted)
[color ]

Off-white
[InChI]

InChI=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
[InChIKey]

IDQUIFLAFFZYEX-UHFFFAOYSA-N
[SMILES]

B(C1=CC=CC(N2C3=C(C=CC=C3)C3=C2C=CC=C3)=C1)(O)O
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H315-H319
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
[HS Code ]

2933998090
Hazard InformationBack Directory
[Chemical Properties]

off-white solid
[Uses]

suzuki 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
Spectrum DetailBack Directory
[Spectrum Detail]

3-(9H-Carbazol-9-yl)phenylboronic acid(864377-33-3)1HNMR
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