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

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.

Specifications

Chemical Identifiers

• CAS: 214360-73-3
• Molecular Formula: C12H18BNO2
• Molecular Weight (g/mol): 219.09
• MDL Number: MFCD02093721
• InChI Key: ZANPJXNYBVVNSD-UHFFFAOYSA-N
• Synonym: 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
• PubChem CID: 2734620
• IUPAC Name: 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
• SMILES: CC1(C)OB(OC1(C)C)C1=CC=C(N)C=C1

• Quantity: 5 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