Cyclohept-1-en-1-ylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a cycloheptene ring. This compound features a seven-membered carbon ring with a double bond, which contributes to its reactivity and potential applications in organic synthesis. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it valuable in various chemical reactions, including Suzuki coupling reactions, which are essential for constructing carbon-carbon bonds in organic chemistry. Cyclohept-1-en-1-ylboronic acid is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Its reactivity is influenced by the presence of the double bond and the boron atom, which can participate in nucleophilic and electrophilic reactions. This compound is of interest in medicinal chemistry and materials science due to its potential applications in drug development and the synthesis of complex organic molecules. Proper handling and storage are essential, as boronic acids can be sensitive to moisture and air.

cyclohept-1-en-1-ylboronic acid

835882-35-4: Cyclohept-1-en-1-ylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a cycloheptene ring. This compound features a seven-membered carbon ring with a double bond, which contributes to its reactivity and potential applications in organic synthesis. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it valuable in various chemical reactions, including Suzuki coupling reactions, which are essential for constructing carbon-carbon bonds in organic chemistry. Cyclohept-1-en-1-ylboronic acid is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Its reactivity is influenced by the presence of the double bond and the boron atom, which can participate in nucleophilic and electrophilic reactions. This compound is of interest in medicinal chemistry and materials science due to its potential applications in drug development and the synthesis of complex organic molecules. Proper handling and storage are essential, as boronic acids can be sensitive to moisture and air.

CAS 835882-35-4

cyclohept-1-en-1-ylboronic acid

Cyclohepten-1-ylboronic acid

Ref: IN-DA003P45

(Cyclohept-1-en-1-yl)boronic acid

Ref: 54-OR13164

Cyclohepten-1-ylboronic Acid

Ref: TR-C987863