Thermo Scientific Chemicals

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

Catalog number: H51666.03
1 g, Each
Thermo Scientific Chemicals

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

Catalog number: H51666.03
1 g, Each
Quantity
Catalog number: H51666.03
also known as H51666-03
Price (USD)
Quantity
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Chemical Identifiers

CAS
214360-73-3
IUPAC Name
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Molecular Formula
C12H18BNO2
InChI Key
ZANPJXNYBVVNSD-UHFFFAOYSA-N
SMILES
CC1(C)OB(OC1(C)C)C1=CC=C(N)C=C1
Appearance (Color)
Off-white to beige
Form
Crystalline solid
Assay (GC)
>97.5%

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.
RUO – Research Use Only

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