Thermo Scientific Chemicals

4-Formylbenzeneboronic acid, 97%, Thermo Scientific Chemicals

Catalog number: B25199.03
1 g, Each
Thermo Scientific Chemicals

4-Formylbenzeneboronic acid, 97%, Thermo Scientific Chemicals

Catalog number: B25199.03
1 g, Each
Quantity
Catalog number: B25199.03
also known as B25199-03
Price (USD)
Price: 39.40
Online price: 33.65
Your price:
Quantity
-

Chemical Identifiers

CAS
87199-17-5
IUPAC Name
(4-formylphenyl)boronic acid
Molecular Formula
C7H7BO3
InChI Key
VXWBQOJISHAKKM-UHFFFAOYSA-N
SMILES
OB(O)C1=CC=C(C=O)C=C1
Appearance (Color)
White to cream or pale yellow
Form
Powder
Assay (Aqueous acid-base Titration)
≥96.0%
Assay (HPLC)
≥96.0%
Identification (FTIR)
Conforms

Description

4-Formylbenzeneboronic acid acts as a reagent used for Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water, copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids, triethylamine-catalyzed three-component Hantzsch condensations, copper-catalyzed nitrations, oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta, palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides, palladium-catalyzed aerobic oxidative cross-coupling reactions. It acts as a reagent used in preparation of sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells, a novel protein synthesis inhibitor active against Gram-positive bacteria.

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-Formylbenzeneboronic acid acts as a reagent used for Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water, copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids, triethylamine-catalyzed three-component Hantzsch condensations, copper-catalyzed nitrations, oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta, palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides, palladium-catalyzed aerobic oxidative cross-coupling reactions. It acts as a reagent used in preparation of sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells, a novel protein synthesis inhibitor active against Gram-positive bacteria.

Solubility
Slightly Soluble in water.

Notes
Air Sensitive. Store away from air and oxidizing agents. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
RUO – Research Use Only

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