CAS 4334-88-7

4-(Ethoxycarbonyl)phenylboronic acid

Description:

4-(Ethoxycarbonyl)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with an ethoxycarbonyl group. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. Its structure features a boron atom bonded to a phenyl group and a hydroxyl group, which imparts acidic properties, allowing it to participate in various chemical reactions, including Suzuki coupling reactions, which are essential in organic synthesis for forming carbon-carbon bonds. The ethoxycarbonyl group enhances its reactivity and solubility, making it useful in medicinal chemistry and materials science. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug delivery systems. Overall, 4-(Ethoxycarbonyl)phenylboronic acid is a versatile compound with significant utility in synthetic organic chemistry and related fields.

Formula: C₉H₁₁BO₄

InChI: InChI=1S/C9H11BO4/c1-2-14-9(11)7-3-5-8(6-4-7)10(12)13/h3-6,12-13H,2H2,1H3

InChI key: InChIKey=ZLNFACCFYUFTLD-UHFFFAOYSA-N

SMILES: C(OCC)(=O)C1=CC=C(B(O)O)C=C1

Synonyms:

• (4-(Ethoxycabonyl)phenyl)boronic acid
• 4-(Ethoxycarbonyl)phenylboronic acid
• 4-(Ethoxylcarbonyl)phenylboronic acid
• 4-Carboethoxybenzeneboronic acid
• 4-Ethoxy carbonyl phenylboronic acid:
• 4-Ethoxycarbonylphenylboronic acid
• Benzoic acid, 4-borono-, 1-ethyl ester
• Benzoic acid, p-borono-, 1-ethyl ester
• Benzoic acid, p-borono-, ethyl ester
• Ethyl 4-Boronobenzoat
• Ethyl 4-boronobenzoate
• Ethyl 4-dihydroxyborylbenzoate
• [4-[(Ethyloxy)carbonyl]phenyl]boronic acid

4-(Ethoxycarbonyl)benzeneboronic acid, 94%

CAS: 4334-88-7

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

Formula: C₉H₁₁BO₄

Purity: 94%

Color and Shape: White, Crystals or powder or crystalline powder

Molecular weight: 193.99

Ref: 02-H26356

4-Ethoxycarbonylphenylboronic acid

CAS: 4334-88-7

Formula: C₉H₁₁BO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 193.9922

Ref: IN-DA0035WD

4-(Ethoxycarbonyl)benzeneboronic acid

CAS: 4334-88-7

4-(Ethoxycarbonyl)benzeneboronic acid

Formula: C₉H₁₁BO₄

Purity: ≥95%

Color and Shape: white crystalline solid

Molecular weight: 193.99g/mol

Ref: 54-OR10470

4-Ethoxycarbonylphenylboronic acid

CAS: 4334-88-7

Formula: C₉H₁₁BO₄

Molecular weight: 193.99

Ref: 7W-GK7579

4-(Ethoxycarbonyl)phenylboronic Acid (contains varying amounts of Anhydride)

CAS: 4334-88-7

Formula: C₉H₁₁BO₄

Color and Shape: White to Almost white powder to crystal

Molecular weight: 193.99

Ref: 3B-E0868

4-Ethoxycarbonylphenylboronic acid

CAS: 4334-88-7

Formula: C₉H₁₁BO₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 193.99

Ref: 10-F010792

4-(Ethoxycarbonyl)phenylboronic acid

CAS: 4334-88-7

4-(Ethoxycarbonyl)phenylboronic acid is a potential use for picric acid detection. It has been shown to be a chemosensor with an electrochemical impedance spectroscopy response that is sensitive to chloride ions. 4-(Ethoxycarbonyl)phenylboronic acid can be used as a linker in multigram-scale synthesis of aryl halides, and its reaction mechanism has been elucidated by crystal x-ray diffraction. The synthesis of this compound is scalable and involves the formation of an apical carboxylate from ethoxycarbonyl phenyl boronic acid and an aryl halide.

Formula: C₉H₁₁BO₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 193.99 g/mol

Ref: 3D-FE22888