3-(Cyclopropylmethyl)thiophenylboronic 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, including organic synthesis and medicinal chemistry. The compound features a thiophene ring, which contributes to its aromatic properties and potential electronic interactions. The cyclopropylmethyl group adds steric hindrance and may influence the compound's reactivity and solubility. Typically, boronic acids like this one are utilized in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds. The presence of the thiophene moiety may also impart unique electronic properties, making it a candidate for applications in organic electronics or as a building block in drug discovery. Overall, the structural characteristics of 3-(cyclopropylmethyl)thiophenylboronic acid suggest it has potential utility in both synthetic and pharmaceutical chemistry, although specific reactivity and stability would depend on the surrounding conditions and functional groups present in a given reaction context.

3-(CYCLOPROPYLMETHYL)THIOPHENYLBORONIC ACID

1025746-82-0: 3-(Cyclopropylmethyl)thiophenylboronic 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, including organic synthesis and medicinal chemistry. The compound features a thiophene ring, which contributes to its aromatic properties and potential electronic interactions. The cyclopropylmethyl group adds steric hindrance and may influence the compound's reactivity and solubility. Typically, boronic acids like this one are utilized in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds. The presence of the thiophene moiety may also impart unique electronic properties, making it a candidate for applications in organic electronics or as a building block in drug discovery. Overall, the structural characteristics of 3-(cyclopropylmethyl)thiophenylboronic acid suggest it has potential utility in both synthetic and pharmaceutical chemistry, although specific reactivity and stability would depend on the surrounding conditions and functional groups present in a given reaction context.

3-(Cyclopropylmethyl)thiophenylboronic acid

3-[(Cyclopropylmethyl)thio]benzeneboronic acid

CAS 1025746-82-0

3-(CYCLOPROPYLMETHYL)THIOPHENYLBORONIC ACID

3-(Cyclopropylmethyl)thiophenylboronic acid

Ref: IN-DA0007SS

3-[(Cyclopropylmethyl)thio]benzeneboronic acid

Ref: 54-OR360165