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  7. 4-Aminobenzeneboronic acid pinacol ester, 98%, Thermo Scientific Chemicals

4-Aminobenzeneboronic acid pinacol ester, 98%, Thermo Scientific Chemicals

Catalog Number p-7034021
Click to view available options
Quantity:
1 g
5 g
214360-73-3
C12H18BNO2
219.09
MFCD02093721
ZANPJXNYBVVNSD-UHFFFAOYSA-N
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
2734620
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
CC1(C)OB(OC1(C)C)C1=CC=C(N)C=C1
214360-73-3
C12H18BNO2
219.09
MFCD02093721
ZANPJXNYBVVNSD-UHFFFAOYSA-N
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
2734620
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
CC1(C)OB(OC1(C)C)C1=CC=C(N)C=C1

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.

Applications
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.

Solubility
Slightly soluble in water.

Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
TRUSTED_SUSTAINABILITY
Quantity 1 g
Solubility Information Slightly soluble in water.
Formula Weight 219.09
Percent Purity 98%
Chemical Name or Material 4-Aminobenzeneboronic acid pinacol ester

Safety and Handling

Hazard Category H315-H319-H335
Precautionary Statement P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
TSCA No
Recommended Storage Ambient temperatures
SDS

RUO – Research Use Only

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