2-Bromo-2,3,3,3-tetrafluoropropionic acid is a fluorinated organic compound characterized by the presence of both bromine and multiple fluorine atoms attached to a propionic acid backbone. Its molecular structure features a bromine atom at the second carbon position and four fluorine atoms at the 2, 3, and 3 positions, contributing to its unique reactivity and properties. This compound is typically a colorless liquid or solid, depending on the temperature, and is known for its strong acidity due to the carboxylic acid functional group. The presence of electronegative fluorine atoms significantly influences its chemical behavior, enhancing its acidity and making it a useful reagent in various organic synthesis applications. Additionally, the bromine atom can participate in nucleophilic substitution reactions, further expanding its utility in chemical transformations. Due to its fluorinated nature, this compound may exhibit distinct physical properties, such as low volatility and high stability under certain conditions, making it of interest in both industrial and research settings. Safety precautions are necessary when handling this compound due to its potential environmental and health impacts.

2-BROMO-2,3,3,3-TETRAFLUOROPROPIONIC ACID

13859-31-9: 2-Bromo-2,3,3,3-tetrafluoropropionic acid is a fluorinated organic compound characterized by the presence of both bromine and multiple fluorine atoms attached to a propionic acid backbone. Its molecular structure features a bromine atom at the second carbon position and four fluorine atoms at the 2, 3, and 3 positions, contributing to its unique reactivity and properties. This compound is typically a colorless liquid or solid, depending on the temperature, and is known for its strong acidity due to the carboxylic acid functional group. The presence of electronegative fluorine atoms significantly influences its chemical behavior, enhancing its acidity and making it a useful reagent in various organic synthesis applications. Additionally, the bromine atom can participate in nucleophilic substitution reactions, further expanding its utility in chemical transformations. Due to its fluorinated nature, this compound may exhibit distinct physical properties, such as low volatility and high stability under certain conditions, making it of interest in both industrial and research settings. Safety precautions are necessary when handling this compound due to its potential environmental and health impacts.

2-Bromotetrafluoropropionic acid

2-Bromo-2,3,3,3-tetrafluoropropionic acid

CAS 13859-31-9

2-BROMO-2,3,3,3-TETRAFLUOROPROPIONIC ACID

2-Bromotetrafluoropropionic acid

Ref: IN-DA0018TU

2-Bromo-2,3,3,3-tetrafluoropropionic acid

Ref: 54-PC5515