CAS 221037-98-5: 3-iodophenylboronic acid

Description: 3-Iodophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that also contains an iodine substituent at the meta position. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the boronic acid group. It exhibits properties typical of boronic acids, including the ability to form reversible complexes with diols, which makes it useful in various applications, particularly in organic synthesis and medicinal chemistry. The iodine atom enhances its reactivity and can facilitate further functionalization or coupling reactions, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, 3-iodophenylboronic acid can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a widely used method for forming carbon-carbon bonds in organic synthesis. Its unique combination of functional groups allows for diverse applications in chemical research and development.

Formula: C₆H₆BIO₂

InChI: InChI=1/C6H6BIO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4,9-10H

3-Iodobenzeneboronic acid, 97%

CAS: 221037-98-5

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. …

• Formula: C₆H₆BIO₂
• Purity: 97%
• Molecular weight: 247.83

Boronic acid, (3-iodophenyl)-

CAS: 221037-98-5

• Formula: C₆H₆BIO₂
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 247.8261

3-Iodophenylboronic acid

CAS: 221037-98-5

• Purity: 97+%
• Molecular weight: 247.83g/mol

3-Iodophenylboronic acid

CAS: 221037-98-5

• Purity: 97.0%
• Color and Shape: Solid
• Molecular weight: 247.8300018310547

3-Iodophenylboronic acid

CAS: 221037-98-5

3-Iodophenylboronic acid is a boronate reagent that is used in the synthesis of pharmaceuticals, such …

• Formula: C₆H₆BIO₂
• Purity: Min. 95%
• Molecular weight: 247.83 g/mol