CAS 2377611-46-4

2-(Ethoxycarbonyl)-1-benzothiophene-4-boronic acid

Description:

2-(Ethoxycarbonyl)-1-benzothiophene-4-boronic acid is a chemical compound that features a benzothiophene core, which is a fused ring structure containing both benzene and thiophene moieties. This compound is characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various organic synthesis applications, particularly in Suzuki coupling reactions. The ethoxycarbonyl group contributes to its reactivity and solubility properties. Typically, compounds like this are utilized in medicinal chemistry and materials science due to their potential biological activity and ability to participate in cross-coupling reactions. The presence of the boronic acid group also allows for the formation of stable complexes with biomolecules, which can be advantageous in drug development and biochemical research. Overall, this compound exemplifies the intersection of organic chemistry and materials science, showcasing the utility of boronic acids in synthetic methodologies.

Formula: C₁₁H₁₁BO₄S

Synonyms:

• 2-(Ethoxycarbonyl)-1-benzothiophene-4-boronic acid

2-(Ethoxycarbonyl)-1-benzothiophene-4-boronic acid

CAS: 2377611-46-4

Formula: C₁₁H₁₁BO₄S

Purity: 97%

Color and Shape: Solid

Molecular weight: 250.0786

Ref: IN-DA00JMHR

2-(Ethoxycarbonyl)-1-benzothiophene-4-boronic acid

CAS: 2377611-46-4

2-(Ethoxycarbonyl)-1-benzothiophene-4-boronic acid

Purity: 97%

Molecular weight: 250.08g/mol

Ref: 54-OR906554

2-(Ethoxycarbonyl)-1-benzothiophene-4-boronic acid

CAS: 2377611-46-4

Purity: 97%

Molecular weight: 250.0800018

Ref: 10-F622886