3-Chloro-4-(cyclopropylmethoxy)phenylboronic 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 such as organic synthesis and medicinal chemistry. The compound features a chlorinated phenyl ring, which can influence its reactivity and solubility, as well as a cyclopropylmethoxy substituent that may enhance its biological activity or selectivity. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This compound may exhibit properties such as moderate to high polarity due to the presence of the boronic acid and ether functionalities, and it may be soluble in polar organic solvents. Its unique structure suggests potential applications in drug development, particularly in the design of inhibitors or modulators of biological targets. As with many boronic acids, care should be taken in handling due to their sensitivity to moisture and air, which can affect their stability and reactivity.

3-Chloro-4-(cyclopropylMethoxy)phenylboronic acid

1228181-35-8: 3-Chloro-4-(cyclopropylmethoxy)phenylboronic 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 such as organic synthesis and medicinal chemistry. The compound features a chlorinated phenyl ring, which can influence its reactivity and solubility, as well as a cyclopropylmethoxy substituent that may enhance its biological activity or selectivity. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This compound may exhibit properties such as moderate to high polarity due to the presence of the boronic acid and ether functionalities, and it may be soluble in polar organic solvents. Its unique structure suggests potential applications in drug development, particularly in the design of inhibitors or modulators of biological targets. As with many boronic acids, care should be taken in handling due to their sensitivity to moisture and air, which can affect their stability and reactivity.

CAS 1228181-35-8

3-Chloro-4-(cyclopropylMethoxy)phenylboronic acid

3-Chloro-4-(cyclopropylmethoxy)phenylboronic acid

Ref: IN-DA009WTP

3-Chloro-4-(cyclopropylmethoxy)phenylboronic acid

Ref: 54-OR360921

3-Chloro-4-(cyclopropylmethoxy)phenylboronic acid

Ref: 10-F623501