3-(Methoxycarbonyl)benzeneboronic acid, 97%
3-(Methoxycarbonyl)benzeneboronic acid, 97%
3-(Methoxycarbonyl)benzeneboronic acid, 97%
Thermo Scientific Chemicals

3-(Methoxycarbonyl)benzeneboronic acid, 97%

CAS: 99769-19-4 | C8H9BO4 | 179.97 g/mol
Quantity:
1 g
5 g
Catalog number H27444.03
also known as H27444-03
Price (JPY)
-
Quantity:
1 g
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Chemical Identifiers
CAS99769-19-4
IUPAC Name[3-(methoxycarbonyl)phenyl]boronic acid
Molecular FormulaC8H9BO4
InChI KeyALTLCJHSJMGSLT-UHFFFAOYSA-N
SMILESCOC(=O)C1=CC=CC(=C1)B(O)O
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SpecificationsSpecification SheetSpecification Sheet
FormPowder
Proton NMRConforms to structure
Assay (Aqueous acid-base Titration)≥96.0%
Appearance (Color)White to pale cream
Assay (HPLC)≥96.0%
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.

Applications
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.

Solubility
Reacts with water.

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

General References:

  1. Kiyofumi Inamoto et. al.Tandem-type Pd(II)-catalyzed oxidative Heck reaction/intramolecular C-H amidation sequence: a novel route to 4-aryl-2-quinolinones.. Chemical Communications. 2012, 48(36),4332-4334.
  2. Qingqing Qi et. al. Copper-mediated aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides at room temperature. Journal of the American Chemical Society. 2012 , 134 (15), 6548-6551.