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3-(Methoxycarbonyl)benzeneboronic acid, 97%, Thermo Scientific Chemicals
$102.82 - $289.60
Chemical Identifiers
CAS | 99769-19-4 |
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Molecular Formula | C8H9BO4 |
Molecular Weight (g/mol) | 179.97 |
MDL Number | MFCD02093046 |
InChI Key | ALTLCJHSJMGSLT-UHFFFAOYSA-N |
Synonym | 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 |
Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
AAH2744403
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Thermo Scientific Chemicals
H2744403 |
1 g |
Each for $102.82
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AAH2744406
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Thermo Scientific Chemicals
H2744406 |
5 g |
Each for $289.60
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Description
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.
ApplicationsReagent 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.
Chemical Identifiers
99769-19-4 | |
179.97 | |
ALTLCJHSJMGSLT-UHFFFAOYSA-N | |
2734714 |
C8H9BO4 | |
MFCD02093046 | |
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 | |
COC(=O)C1=CC=CC(=C1)B(O)O |
Specifications
99769-19-4 | |
C8H9BO4 | |
1 g | |
Reacts with water. | |
COC(=O)C1=CC=CC(=C1)B(O)O | |
179.97 | |
179.97 | |
3-(Methoxycarbonyl)benzeneboronic acid |
136°C | |
MFCD02093046 | |
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 | |
ALTLCJHSJMGSLT-UHFFFAOYSA-N | |
[3-(methoxycarbonyl)phenyl]boronic acid | |
2734714 | |
97% |
Safety and Handling
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only