trans-2,3-Dibromo-2-butene-1,4-diol CAS:3234-02-4

trans-2,3-Dibromo-2-butene-1,4-diol is a halogenated organic compound characterized by its unique structure, which includes a butene backbone with bromine substitutions at carbons 2 and 3, along with hydroxyl (-OH) groups at the terminal positions. Its molecular formula is C4H6Br2O2, and the compound’s trans configuration significantly influences its reactivity and interactions with other molecules. The presence of the bromine atoms introduces significant electrophilic character to the molecule, making it useful in various synthetic applications. The bromines can serve as leaving groups in nucleophilic substitution reactions, enabling the formation of new carbon-nucleophile bonds. This property makes trans-2,3-dibromo-2-butene-1,4-diol a valuable intermediate in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and specialty chemicals. Additionally, the hydroxyl groups contribute to the compound's solubility in polar solvents and allow it to engage in hydrogen bonding. This characteristic enhances the compound's utility in organic synthesis, where it can undergo reactions typical of alcohols, such as dehydration or oxidation. As a result, trans-2,3-dibromo-2-butene-1,4-diol can be transformed into various derivatives through targeted modifications. Moreover, this compound can be employed in studies related to brominated compounds, contributing to research in areas like material science and polymer chemistry. Brominated substances often exhibit unique properties that can be leveraged for flame retardancy and enhancing thermal stability in polymers. While trans-2,3-dibromo-2-butene-1,4-diol demonstrates considerable utility, its handling requires caution due to the presence of bromine, which can pose health risks upon exposure. Proper laboratory practices, including the use of personal protective equipment (PPE), are essential when working with this compound. In summary, trans-2,3-dibromo-2-butene-1,4-diol is a multifunctional compound with diverse applications in organic synthesis and research, highlighting its significance in advancing chemical science while necessitating careful handling to ensure safety.