(5-(4-Chlorophenyl)thiophen-2-yl)boronic acid is an organoboron compound 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 applications, particularly in organic synthesis and medicinal chemistry. The compound features a thiophene ring, which contributes to its aromatic properties and potential electronic characteristics. The presence of a 4-chlorophenyl substituent enhances its reactivity and solubility in organic solvents. This compound is typically used in Suzuki coupling reactions, a widely employed method for forming carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, boronic acids like this one can serve as intermediates in the development of sensors and materials due to their unique reactivity and ability to interact with biological molecules. Overall, (5-(4-chlorophenyl)thiophen-2-yl)boronic acid is a versatile compound with significant implications in both research and industrial applications.

(5-(4-chlorophenyl)thiophen-2-yl)boronic acid

1210470-48-6: (5-(4-Chlorophenyl)thiophen-2-yl)boronic acid is an organoboron compound 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 applications, particularly in organic synthesis and medicinal chemistry. The compound features a thiophene ring, which contributes to its aromatic properties and potential electronic characteristics. The presence of a 4-chlorophenyl substituent enhances its reactivity and solubility in organic solvents. This compound is typically used in Suzuki coupling reactions, a widely employed method for forming carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, boronic acids like this one can serve as intermediates in the development of sensors and materials due to their unique reactivity and ability to interact with biological molecules. Overall, (5-(4-chlorophenyl)thiophen-2-yl)boronic acid is a versatile compound with significant implications in both research and industrial applications.

CAS 1210470-48-6

(5-(4-chlorophenyl)thiophen-2-yl)boronic acid

[5-(4-Chlorophenyl)thiophen-2-yl]boronic acid

Ref: IN-DA008TKU

(5-(4-chlorophenyl)thiophen-2-yl)boronic acid

Ref: 54-OR1034574

(5-(4-chlorophenyl)thiophen-2-yl)boronic acid

Ref: 10-F988930