2,2,2-Trifluoroethyl 2-fluoroprop-2-enoate is an organic compound characterized by its unique fluorinated structure, which significantly influences its chemical properties. This substance features a trifluoroethyl group, contributing to its high electronegativity and making it a polar molecule. The presence of the 2-fluoroprop-2-enoate moiety introduces a vinyl group, which can participate in various chemical reactions, including polymerization and addition reactions. The compound is typically a colorless liquid at room temperature and may have a low boiling point due to its relatively small molecular size. Its fluorinated nature imparts stability against hydrolysis and enhances its lipophilicity, making it useful in various applications, including as an intermediate in organic synthesis and in the production of fluorinated polymers. Additionally, the compound's reactivity can be influenced by the presence of the double bond, allowing for further functionalization. Safety precautions should be taken when handling this compound, as fluorinated compounds can exhibit toxicity and environmental persistence.

2,2,2-trifluoroethyl 2-fluoroprop-2-enoate

74359-10-7: 2,2,2-Trifluoroethyl 2-fluoroprop-2-enoate is an organic compound characterized by its unique fluorinated structure, which significantly influences its chemical properties. This substance features a trifluoroethyl group, contributing to its high electronegativity and making it a polar molecule. The presence of the 2-fluoroprop-2-enoate moiety introduces a vinyl group, which can participate in various chemical reactions, including polymerization and addition reactions. The compound is typically a colorless liquid at room temperature and may have a low boiling point due to its relatively small molecular size. Its fluorinated nature imparts stability against hydrolysis and enhances its lipophilicity, making it useful in various applications, including as an intermediate in organic synthesis and in the production of fluorinated polymers. Additionally, the compound's reactivity can be influenced by the presence of the double bond, allowing for further functionalization. Safety precautions should be taken when handling this compound, as fluorinated compounds can exhibit toxicity and environmental persistence.

CAS 74359-10-7

2,2,2-trifluoroethyl 2-fluoroprop-2-enoate

2,2,2-Trifluoroethyl-2-fluoroacrylate

Ref: 54-PC4975