2,2,3,3-Tetrafluoropropyl 2-fluoroprop-2-enoate is a fluorinated organic compound characterized by its unique structure, which includes multiple fluorine atoms and an ester functional group. This compound typically exhibits high thermal stability and low volatility due to the presence of fluorine, which enhances its resistance to degradation. The fluorinated groups contribute to its hydrophobic nature, making it less soluble in water but potentially soluble in organic solvents. Its reactivity is influenced by the presence of the double bond in the prop-2-enoate moiety, allowing for potential participation in various chemical reactions, such as polymerization or nucleophilic addition. Additionally, the compound may exhibit unique physical properties, such as altered boiling and melting points compared to non-fluorinated analogs. Due to its specific structure, it may find applications in specialized fields, including materials science and pharmaceuticals, where fluorinated compounds are often valued for their unique chemical and physical properties. Safety and handling precautions should be observed, as with all fluorinated compounds, due to potential toxicity and environmental concerns.

2,2,3,3-tetrafluoropropyl 2-fluoroprop-2-enoate

96250-37-2: 2,2,3,3-Tetrafluoropropyl 2-fluoroprop-2-enoate is a fluorinated organic compound characterized by its unique structure, which includes multiple fluorine atoms and an ester functional group. This compound typically exhibits high thermal stability and low volatility due to the presence of fluorine, which enhances its resistance to degradation. The fluorinated groups contribute to its hydrophobic nature, making it less soluble in water but potentially soluble in organic solvents. Its reactivity is influenced by the presence of the double bond in the prop-2-enoate moiety, allowing for potential participation in various chemical reactions, such as polymerization or nucleophilic addition. Additionally, the compound may exhibit unique physical properties, such as altered boiling and melting points compared to non-fluorinated analogs. Due to its specific structure, it may find applications in specialized fields, including materials science and pharmaceuticals, where fluorinated compounds are often valued for their unique chemical and physical properties. Safety and handling precautions should be observed, as with all fluorinated compounds, due to potential toxicity and environmental concerns.

2,2,3,3-Tetrafluoropropyl-2'-fluoroacrylate

CAS 96250-37-2

2,2,3,3-tetrafluoropropyl 2-fluoroprop-2-enoate

2,2,3,3-Tetrafluoropropyl-2'-fluoroacrylate

Ref: 54-PC4973

2,2,3,3-Tetrafluoropropyl 2-fluoroacrylate

Ref: 10-F010470