DIBENZOFURAN-4-BORONIC ACID

DIBENZOFURAN-4-BORONIC ACID Basic information
Product Name:DIBENZOFURAN-4-BORONIC ACID
Synonyms:RARECHEM AH PB 0052;TIMTEC-BB SBB003426;DIBENZOFURAN-4-BORONIC ACID;AKOS BRN-0085;Dibenzofuran-4-boronic acid, 98+%;4-(Dibenzofuranyl)boronic acid;nzofuran-4-Boronic acid;4-dibenzofuran boronic
CAS:100124-06-9
MF:C12H9BO3
MW:212.01
EINECS:672-293-9
Product Categories:Heterocyclic Compounds;Boronic acid;Dibenzofuran;Organoborons;Boronic Acids;Boronic Acids and Derivatives;Heteroaryl;OLED materials,pharm chemical,electronic;100124-06-9
Mol File:100124-06-9.mol
DIBENZOFURAN-4-BORONIC ACID Structure
DIBENZOFURAN-4-BORONIC ACID Chemical Properties
Melting point 286-291 °C (lit.)
Boiling point 438.5±37.0 °C(Predicted)
density 1.34±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka8.04±0.30(Predicted)
form powder
color white to off-white
BRN 1645426
InChIKeyZXHUJRZYLRVVNP-UHFFFAOYSA-N
CAS DataBase Reference100124-06-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 37/39-26-24/25
WGK Germany 3
TSCA No
HazardClass IRRITANT
HS Code 29321900
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
DIBENZOFURAN-4-BORONIC ACID Usage And Synthesis
DescriptionDibenzofuran-4-boronic acid (DBFBA) is a boronic acid that has been used as a cross-coupling agent in the Suzuki coupling reaction. It has been shown to have low efficiency, but advances in this area have been made through the use of methanol extraction and photophysical properties. DBFBA is often coupled with imidazole derivatives to form anti-inflammatory compounds. The bond cleavage and hydrogen bonding properties of DBFBA make it a good target for drug synthesis.
Chemical Propertiesoff-white to beige powder
SynthesisIn a 300 ml three-necked flask, 7.2 g of 4-bromodibenzofuran was dissolved in -78° C. anhydrous tetrahydrofuran (THF) under an argon atmosphere. Then, 20 ml of an n-butyl lithium-n-hexane solution (1.6 M, 1.1 eq) was added and stirred for 1 hour. 4.23 ml (1.3 eq) of trimethoxyborane (B(OMe)3) was added and stirred for 2 hours, and the temperature of the reaction system was increased to room temperature. 200 ml of 1 N hydrochloric acid was added into the reactant and stirred for 3 hours. An organic layer was separated, and solvents were distilled off. In the crude product thus obtained, hexane was added. Precipitated product was filtered to obtain 4.94 g of dibenzofuran-4-boronic acid as a white solid (yield 80%).
DIBENZOFURAN-4-BORONIC ACID Preparation Products And Raw materials
Preparation ProductsBoronic acid, B-(6-phenyl-4-dibenzofuranyl)--->1-bromo-dibenzofuran-4-ol-->4-(2-bromophenyl)dibenzo[b,d]furan
DIBENZOFURAN-2-CARBOXALDEHYDE 4-Bromophenoxybenzene dibenzo[b,d]furan-3-ylboronic acid 4-BROMO-P-TERPHENYL Dibenzo[b,d]furan-2-ylboronic acid 4-Bromodiphenylamine 5-Chloro-2-fluoropyridin-3-ylboronic acid DIBENZOFURAN-4-CARBOXALDEHYDE 97 2-Chloro-3-pyridylboronic acid 4-DIBENZOTHIOPHENEBORONIC ACID 2-Fluoro-3-pyridylboronic acid 4-(DIMETHOXYMETHYL)-2-METHYLPYRIMIDINE 4-AMINO-N,N-DIMETHYLBENZYLAMINE 4-Chlorobiphenyl Dibenzofuran DIBENZOFURAN-4-BORONIC ACID Methylboronic acid Phenylboronic acid

Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.