Trans-3-Bromot-2-(2-propynyloxy)-tetrahydrofuran is a chemical compound characterized by its unique structure, which includes a tetrahydrofuran ring with a bromine atom and a propynyloxy substituent. The presence of the bromine atom introduces reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The tetrahydrofuran ring contributes to the compound's cyclic ether properties, which can influence its solubility and reactivity in organic solvents. The propynyloxy group adds a degree of steric hindrance and can affect the compound's overall polarity and interaction with other molecules. This compound may be of interest in synthetic organic chemistry, particularly in the development of pharmaceuticals or agrochemicals, due to its functional groups that can participate in further chemical transformations. Additionally, the trans configuration of the bromine and propynyloxy groups can impact the compound's stereochemistry, influencing its biological activity and reactivity. Overall, trans-3-Bromot-2-(2-propynyloxy)-tetrahydrofuran presents a versatile framework for further chemical exploration.

trans-3-Bromot-2-(2-propynyloxy)-etrahydrofuran

109789-15-3: Trans-3-Bromot-2-(2-propynyloxy)-tetrahydrofuran is a chemical compound characterized by its unique structure, which includes a tetrahydrofuran ring with a bromine atom and a propynyloxy substituent. The presence of the bromine atom introduces reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The tetrahydrofuran ring contributes to the compound's cyclic ether properties, which can influence its solubility and reactivity in organic solvents. The propynyloxy group adds a degree of steric hindrance and can affect the compound's overall polarity and interaction with other molecules. This compound may be of interest in synthetic organic chemistry, particularly in the development of pharmaceuticals or agrochemicals, due to its functional groups that can participate in further chemical transformations. Additionally, the trans configuration of the bromine and propynyloxy groups can impact the compound's stereochemistry, influencing its biological activity and reactivity. Overall, trans-3-Bromot-2-(2-propynyloxy)-tetrahydrofuran presents a versatile framework for further chemical exploration.

<p>Applications (+/-)-trans-3-Bromotetrahydro-2-(2-propynyloxy)-furan (cas# 109789-15-3) is a compound useful in organic synthesis.<br></p>

CAS 109789-15-3

trans-3-Bromot-2-(2-propynyloxy)-etrahydrofuran

(+/-)-trans-3-Bromotetrahydro-2-(2-propynyloxy)-furan

Ref: TR-B688040