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  7. 4-(Ethoxycarbonyl)benzeneboronic acid, 94%, Thermo Scientific Chemicals

4-(Ethoxycarbonyl)benzeneboronic acid, 94%, Thermo Scientific Chemicals

Catalog Number p-7028939
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Quantity:
1 g
5 g
This item is not returnable. View return policy
4334-88-7
C9H11BO4
193.99
MFCD02179441
ZLNFACCFYUFTLD-UHFFFAOYSA-N
4-ethoxycarbonylphenyl boronic acid, 4-ethoxycarbonyl phenylboronic acid, 4-ethoxycarbonyl phenyl boronic acid, 4-ethoxycarbonyl benzeneboronic acid, 4-ethoxycarbonylbenzeneboronic acid, ethyl 4-boronobenzoate, p-ethoxycarbonylphenylboronic acid, ethyl 4-dihydroxyboranyl benzoate, 4-carbethoxyphenylboronic acid, benzoic acid, 4-borono-, 1-ethyl ester
2734350
(4-ethoxycarbonylphenyl)boronic acid
CCOC(=O)C1=CC=C(C=C1)B(O)O
This item is not returnable. View return policy
4334-88-7
C9H11BO4
193.99
MFCD02179441
ZLNFACCFYUFTLD-UHFFFAOYSA-N
4-ethoxycarbonylphenyl boronic acid, 4-ethoxycarbonyl phenylboronic acid, 4-ethoxycarbonyl phenyl boronic acid, 4-ethoxycarbonyl benzeneboronic acid, 4-ethoxycarbonylbenzeneboronic acid, ethyl 4-boronobenzoate, p-ethoxycarbonylphenylboronic acid, ethyl 4-dihydroxyboranyl benzoate, 4-carbethoxyphenylboronic acid, benzoic acid, 4-borono-, 1-ethyl ester
2734350
(4-ethoxycarbonylphenyl)boronic acid
CCOC(=O)C1=CC=C(C=C1)B(O)O

Description

4-(Ethoxycarbonyl)benzeneboronic acid is used as a reactant involved in oxidative hydroxylation for the preparation of phenols, homolytic aromatic substitution, cross-coupling with α-bromocarbonyl compounds, Suzuki-coupling reaction with quinoline carboxylates, trifluoromethylation and carbometalation of ynamides.

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
4-(Ethoxycarbonyl)benzeneboronic acid is used as a reactant involved in oxidative hydroxylation for the preparation of phenols, homolytic aromatic substitution, cross-coupling with α-bromocarbonyl compounds, Suzuki-coupling reaction with quinoline carboxylates, trifluoromethylation and carbometalation of ynamides.

Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
TRUSTED_SUSTAINABILITY
Melting Point 137°C to 140°C
Quantity 1 g
Formula Weight 193.99
Percent Purity 94%
Chemical Name or Material 4-(Ethoxycarbonyl)benzeneboronic acid

RUO – Research Use Only

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