CAS 685514-61-8: Boronic acid, (2,3-dihydro-7-benzofuranyl)-

Description: Boronic acid, (2,3-dihydro-7-benzofuranyl)-, identified by its CAS number 685514-61-8, is an organic compound characterized by the presence of a boronic acid functional group attached to a benzofuran moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The benzofuran structure contributes to its aromatic characteristics, potentially influencing its reactivity and solubility. Boronic acids are known for their role in Suzuki coupling reactions, which are vital in the formation of carbon-carbon bonds in organic synthesis. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Its stability, solubility in organic solvents, and reactivity with nucleophiles are essential characteristics that define its utility in chemical processes. Overall, this compound represents a valuable tool in both synthetic and medicinal chemistry contexts.

Formula: C₈H₉BO₃

(2,3-Dihydrobenzofuran-7-yl)boronic acid

CAS: 685514-61-8

• Formula: C₈H₉BO₃
• Purity: 97%
• Color and Shape: Solid
• Molecular weight: 163.9663

2,3-Dihydro-1-benzofuran-7-boronic acid

CAS: 685514-61-8

• Purity: 97%
• Molecular weight: 163.97g/mol

2,3-Dihydro-1-benzofuran-7-ylboronic acid

CAS: 685514-61-8

• Purity: 95.0%
• Color and Shape: Solid, Light beige powder
• Molecular weight: 163.97000122070312

2,3-Dihydro-1-benzofuran-7-ylboronic acid

CAS: 685514-61-8

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• Formula: C₈H₉BO₃
• Purity: Min. 95%
• Molecular weight: 163.97 g/mol