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

Catalog Number AAH2744406
Click to view available options
Quantity:
1 g
5 g
99769-19-4
C8H9BO4
179.97
MFCD02093046
ALTLCJHSJMGSLT-UHFFFAOYSA-N
3-methoxycarbonyl phenylboronic acid, 3-methoxycarbonylphenyl boronic acid, 3-methoxycarbonyl phenyl boronic acid, 3-methoxycarbonyl benzeneboronic acid, 3-methoxycarbonylphenylbaronic acid, methyl 3-dihydroxyboranyl benzoate, m-methoxycarbonyl phenylboronic acid, 3-carbomethoxy-phenylboronic acid
2734714
COC(=O)C1=CC=CC(=C1)B(O)O
99769-19-4
C8H9BO4
179.97
MFCD02093046
ALTLCJHSJMGSLT-UHFFFAOYSA-N
3-methoxycarbonyl phenylboronic acid, 3-methoxycarbonylphenyl boronic acid, 3-methoxycarbonyl phenyl boronic acid, 3-methoxycarbonyl benzeneboronic acid, 3-methoxycarbonylphenylbaronic acid, methyl 3-dihydroxyboranyl benzoate, m-methoxycarbonyl phenylboronic acid, 3-carbomethoxy-phenylboronic acid
2734714
COC(=O)C1=CC=CC(=C1)B(O)O

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.
TRUSTED_SUSTAINABILITY
Melting Point 136°C
Quantity 5 g
Solubility Information Reacts with water.
IUPAC Name (3-methoxycarbonylphenyl)boronic acid
Formula Weight 179.97
Percent Purity 97%
Chemical Name or Material 3-(Methoxycarbonyl)benzeneboronic acid
Hazard Category H315-H319-H335
Hazard Statement GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Precautionary Statement P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
TSCA No
Recommended Storage Ambient temperatures

RUO – Research Use Only

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