3-(Methoxycarbonyl)benzeneboronic acid, 97%

CAS: 99769-19-4

Ref. 02-H27444

Produktinformation

• Name: 3-(Methoxycarbonyl)benzeneboronic acid, 97%
• Synonyme: 3-(methoxycarbonyl)phenylboronic acid, 3-Methoxycarbonylphenylboronic acid, Methyl 3-Boronobenzoat, 3-(Methyloxycarbonyl)phenylboronic acid, Methyl 3-boronobenzoate, 3-(methoxycarbonyl)Benzeneboronic acid, (3-(Methoxycarbonyl)Phenyl)Boronic Acid, 3-(Methoxycarbonyl)phenylboronic acid, 3-Methoxycarbonylphenylbaronic Acid

Beschreibung

Reagent used for tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence, copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, one-pot ipso-nitration of arylboronic acids, copper-catalyzed nitration, cyclocondensation followed by palladium-phosphine-catalyzed Suzuki-Miyaura coupling. Reagent used in Preparation of biaryls via nickel-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl halides with arylboronic acid6, chromenones and their bradykinin B1 antagonistic active, Pt nanoparticles at Photoactive metal-organic frameworks resulting in efficient hydrogen evolution via synergistic photoexcitation and electron injecti, salicylate-based thienylbenzoic acids as E. coli methionine aminopeptidase inhibitor. 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.

• Marke: Alfa Aesar By Thermo Fisher Scientific

Chemische Eigenschaften

• Molekulargewicht: 179.97
• Formel: C₈H₉BO₄
• Reinheit: 97%
• Farbe/Form: White to pale cream, Powder
• InChI Key: ALTLCJHSJMGSLT-UHFFFAOYSA-N