CAS 113893-08-6

Benzothiophene-3-boronic acid

Description:

Benzothiophene-3-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a benzothiophene ring system. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, including stability and reactivity due to the boronic acid moiety. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it useful in various applications such as Suzuki coupling reactions in organic synthesis. Benzothiophene derivatives often display interesting electronic properties, which can be leveraged in materials science, particularly in organic semiconductors and photovoltaic devices. Additionally, the presence of sulfur in the benzothiophene structure can impart unique chemical reactivity and influence the compound's solubility and interaction with biological systems. Overall, Benzothiophene-3-boronic acid is a versatile compound with potential applications in organic synthesis, medicinal chemistry, and materials science.

Formula: C₈H₇BO₂S

InChI: InChI=1/C8H7BO2S/c10-9(11)7-5-12-8-4-2-1-3-6(7)8/h1-5,10-11H

SMILES: c1ccc2c(c1)c(cs2)B(O)O

Synonyms:

• Akos Brn-0283
• 1-Benzothiophen-3-Ylboronic Acid
• Benzo[B]Thiophene-3-Boronic Acid
• Asdi-Inter 500027787
• Thianaphthene-3-Boronic Acid
• Benzo[b]thiophen-3-yl-boronic acid

Benzo[b]thiophene-3-boronic Acid (contains varying amounts of Anhydride)

CAS: 113893-08-6

Formula: C₈H₇BO₂S

Purity: 97.0 to 112.0 %

Color and Shape: White to Light yellow to Light orange powder to crystal

Molecular weight: 178.01

Ref: 3B-B4774

Boronic acid, B-benzo[b]thien-3-yl-

CAS: 113893-08-6

Formula: C₈H₇BO₂S

Purity: 98%

Color and Shape: Solid

Molecular weight: 178.0160

Ref: IN-DA000A0A

Benzo[b]thiophene-3-boronic acid

CAS: 113893-08-6

Benzo[b]thiophene-3-boronic acid

Formula: C₈H₇BO₂S

Purity: 98%

Color and Shape: white to off-white solid

Molecular weight: 178.02g/mol

Ref: 54-OR23178

1-benzothien-3-ylboronic acid

CAS: 113893-08-6

Formula: C₈H₇BO₂S

Purity: 95%

Color and Shape: Solid

Molecular weight: 178.01

Ref: 10-F308003

Benzo[b]thien-3-ylboronic Acid

Controlled Product

CAS: 113893-08-6

Applications Benzo[b]thien-3-ylboronic acid is used in the synthesis and evaluation of dual wavelength fluorescent benzo[b]thiophene boronic acid derivatives for sugar/glycoprotein sensing.
References Akay, S., et al.: Chem. Biol. Drug Des., 70, 279 (2007)

Formula: C₈H₇BO₂S

Color and Shape: Neat

Molecular weight: 178.02

Ref: TR-B206890

Benzo[b]thiophene-3-boronic acid

CAS: 113893-08-6

Benzo[b]thiophene-3-boronic acid is a boronic acid that can be used in the synthesis of estranes. It is a key intermediate for organic chemists, who use it as a building block for synthesis of organic molecules. This compound can be obtained through electrochemical oxidation of benzo[b]thiophene-3-carboxylic acid with a palladium electrode and an electrolyte solution. The reaction is performed in an evaporator, which removes the solvent and leaves a solid residue. The final product can be purified by recrystallization or distillation. Benzo[b]thiophene-3-boronic acid reacts with electron-rich aromatic compounds to form cross-coupling products, which are often used as ligands in metal complexes.

Formula: C₈H₇BO₂S

Purity: Min. 95%

Molecular weight: 178.02 g/mol

Ref: 3D-FB46198