4-Formylbenzeneboronic acid, 97%

CAS : 87199-17-5

Ref. 02-B25199

Informations sur le produit

• Nom: 4-Formylbenzeneboronic acid, 97%
• Synonymes: 4-formylphenylboronic acid, (4-Formylphenyl)Boronic Acid, 4-Boronobenzaldehyde, 4-Formylbenzeneboronic acid, 4-Formylphenylborate, B-(4-Formylphenyl)boronic acid, Benzeneboronic acid, p-formyl-, Boronic acid, (4-formylphenyl)-, Boronic acid, B-(4-formylphenyl)-, p-Formylbenzeneboronic acid, p-Formylphenylboronic acid

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.

• Marque: Alfa Aesar By Thermo Fisher Scientific

Propriétés chimiques

• Masse moléculaire: 149.94
• Formule: C₇H₇BO₃
• Degré de pureté: 97%
• Couleur/Forme: White to cream or pale yellow, Powder
• Code InChI: VXWBQOJISHAKKM-UHFFFAOYSA-N