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4-Aminobenzeneboronic acid pinacol ester, 98%, Thermo Scientific Chemicals
Supplier: Thermo Scientific Chemicals H5166603
Description
4-Aminobenzeneboronic acid pinacol ester is a reagent used for Suzuki-Miyaura cross-coupling reactions, Mercury(II) detection by fluorometry with new fluorogenic indicators based on through-bond energy transfer from pentaquinone to rhodamine, Rhodium-catalyzed amination reactions and Palladium-catalyzed Suzuki cross-coupling to synthesize potential antitubercular and antimicrobial compounds. It is also used as a reagent in preparation of Hexaphenylbenzene derivatives as a potential bioprobe and multichannel keypad system, Pyromellitic diimide-based polymer as matrix for solution-processable n-channel field-effect transistors, alternating copolymers of oligoarylenes and naphthalene bisimides as low band gap semiconductors with electrochemical and spectroelectrochemical behavior and γ-secretase modulators in the treatment of Amyloid β formation.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications4-Aminobenzeneboronic acid pinacol ester is a reagent used for Suzuki-Miyaura cross-coupling reactions, Mercury(II) detection by fluorometry with new fluorogenic indicators based on through-bond energy transfer from pentaquinone to rhodamine, Rhodium-catalyzed amination reactions and Palladium-catalyzed Suzuki cross-coupling to synthesize potential antitubercular and antimicrobial compounds. It is also used as a reagent in preparation of Hexaphenylbenzene derivatives as a potential bioprobe and multichannel keypad system, Pyromellitic diimide-based polymer as matrix for solution-processable n-channel field-effect transistors, alternating copolymers of oligoarylenes and naphthalene bisimides as low band gap semiconductors with electrochemical and spectroelectrochemical behavior and γ-secretase modulators in the treatment of Amyloid β formation.
Solubility
Slightly soluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
Specifications
4-Aminobenzeneboronic acid pinacol ester | |
C12H18BNO2 | |
1 g | |
Slightly soluble in water. | |
CC1(C)OB(OC1(C)C)C1=CC=C(N)C=C1 | |
219.09 | |
219.09 |
214360-73-3 | |
MFCD02093721 | |
4-aminophenylboronic acid pinacol ester, 4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl aniline, 4-tetramethyl-1,3,2-dioxaborolan-2-yl aniline, 4-aminophenylboronic acid pinacolate, 4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl benzenamine, pinacol cyclic ester, 2-4-aminophenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 4-aminophenylboronic acid, pinacol ester, 4-aminophenylboronicacidpinacolester, 4-aminobenzeneboronic acid pinacol ester | |
ZANPJXNYBVVNSD-UHFFFAOYSA-N | |
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline | |
2734620 | |
98% |
Chemical Identifiers
214360-73-3 | |
219.09 | |
ZANPJXNYBVVNSD-UHFFFAOYSA-N | |
2734620 | |
CC1(C)OB(OC1(C)C)C1=CC=C(N)C=C1 |
C12H18BNO2 | |
MFCD02093721 | |
4-aminophenylboronic acid pinacol ester, 4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl aniline, 4-tetramethyl-1,3,2-dioxaborolan-2-yl aniline, 4-aminophenylboronic acid pinacolate, 4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl benzenamine, pinacol cyclic ester, 2-4-aminophenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 4-aminophenylboronic acid, pinacol ester, 4-aminophenylboronicacidpinacolester, 4-aminobenzeneboronic acid pinacol ester | |
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline |
Safety and Handling
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only