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3-(Methoxycarbonyl)benzeneboronic acid, 97%

Codice prodotto. 11387289
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Codice prodotto. 11387289 Fornitore Thermo Scientific Alfa Aesar N. del fornitore H27444.03
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CAS: 99769-19-4 | C8H9BO4 | 179.97 g/mol

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

Identificatori chimici

CAS 99769-19-4
Formula molecolare C8H9BO4
Molecular Weight (g/mol) 179.97
Numero MDL MFCD02093046
InChI Key ALTLCJHSJMGSLT-UHFFFAOYSA-N
Sinonimo 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
PubChem CID 2734714
SMILES COC(=O)C1=CC=CC(=C1)B(O)O

Specifica

Materiale o nome chimico 3-(Methoxycarbonyl)benzeneboronic acid
Punto di fusione 136°C
Quantità 1 g
Informazioni di solubilità Reacts with water.
IUPAC Name [3-(methoxycarbonyl)phenyl]boronic acid
Peso formulazione 179.97
Percent Purity 97%

RUO – Research Use Only

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