CAS 359012-63-8

Boronic acid, 3-fluoranthenyl-

Description:

Boronic acid, 3-fluoranthenyl- (CAS 359012-63-8) is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a fluoranthenyl moiety. This compound typically exhibits properties associated with both boronic acids and polycyclic aromatic hydrocarbons. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them useful in various applications, including organic synthesis and materials science. The fluoranthenyl group contributes to the compound's aromaticity and potential electronic properties, which may be leveraged in organic electronics or photonic applications. Additionally, boronic acids can participate in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds, which is valuable in the synthesis of complex organic molecules. The compound's solubility, stability, and reactivity can vary based on its specific structure and substituents, influencing its utility in research and industrial applications. Overall, boronic acid, 3-fluoranthenyl- represents a versatile building block in organic chemistry.

Formula: C₁₆H₁₁BO₂

Synonyms:

• Fluoranthene-3-boronic acid

Fluoranthen-3-ylboronic acid

CAS: 359012-63-8

Formula: C₁₆H₁₁BO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 246.0683

Ref: IN-DA003QLO

Fluoranthen-3-ylboronic acid

CAS: 359012-63-8

Fluoranthen-3-ylboronic acid

Purity: 98%

Molecular weight: 246.07g/mol

Ref: 54-OR51016

Fluoranthen-3-ylboronic acid

CAS: 359012-63-8

Formula: C₁₆H₁₁BO₂

Purity: 97%

Molecular weight: 246.07

Ref: 10-F328651