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4-Formylbenzeneboronic acid, 97%, Thermo Scientific Chemicals

Catalog Number 11420678
Click to view available options
Quantity:
1 g
5 g
25 g
87199-17-5
C7H7BO3
149.94
MFCD00151823
VXWBQOJISHAKKM-UHFFFAOYSA-N
4-formylphenyl boronic acid, 4-formylbenzeneboronic acid, 4-boronobenzaldehyde, boronic acid, 4-formylphenyl, boronic acid, b-4-formylphenyl, p-formylphenylboronic acid, 4-dihydroxyboryl benzaldehyde, 4-dihydroxyboranyl benzaldehyde, 4-benzaldehyde boronic acid, 4-formyl-phenylboronic acid
591073
(4-formylphenyl)boronic acid
OB(O)C1=CC=C(C=O)C=C1
87199-17-5
C7H7BO3
149.94
MFCD00151823
VXWBQOJISHAKKM-UHFFFAOYSA-N
4-formylphenyl boronic acid, 4-formylbenzeneboronic acid, 4-boronobenzaldehyde, boronic acid, 4-formylphenyl, boronic acid, b-4-formylphenyl, p-formylphenylboronic acid, 4-dihydroxyboryl benzaldehyde, 4-dihydroxyboranyl benzaldehyde, 4-benzaldehyde boronic acid, 4-formyl-phenylboronic acid
591073
(4-formylphenyl)boronic acid
OB(O)C1=CC=C(C=O)C=C1

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.
TRUSTED_SUSTAINABILITY
Melting Point 260°C to 266°C
Quantity 5 g
Beilstein 3030770
Sensitivity Air Sensitive
Solubility Information Slightly Soluble in water.
Formula Weight 149.94
Percent Purity 97%
Chemical Name or Material 4-Formylbenzeneboronic acid

RUO – Research Use Only

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