Description:5-Acetylthiophene-2-boronic acid is an organoboron compound characterized by the presence of both a boronic acid functional group and a thiophene ring. The molecular structure features a thiophene ring substituted at the 2-position with a boronic acid group and at the 5-position with an acetyl group. This compound is typically used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is valuable for forming carbon-carbon bonds. The boronic acid moiety allows for the formation of stable complexes with diols, making it useful in various applications, including drug discovery and materials science. Additionally, the presence of the acetyl group can influence the reactivity and solubility of the compound. 5-Acetylthiophene-2-boronic acid is generally handled with care due to the reactivity of boronic acids, and it is important to store it under appropriate conditions to maintain its stability.
We use cookies to enhance your visit. We do not include advertising.
Please see our Cookies Policy for more details or adjust your preferences in "Settings".
This is the advanced settings system for our own and third-party cookies. Here you can modify parameters that will directly affect your browsing experience on this website. If you wish you may check the list of Cookie types.
Please note that disabling cookies can cause failures in the normal operation of the web.
