1,1,2-Trifluorobut-1-ene is a fluorinated organic compound characterized by its unsaturated structure, featuring a double bond between the first and second carbon atoms of a four-carbon chain. The presence of three fluorine atoms, specifically at the first and second carbon positions, significantly influences its chemical properties, making it a highly polar molecule with unique reactivity patterns. This compound is typically colorless and may have a faint odor. It is known for its applications in the synthesis of various fluorinated chemicals and as an intermediate in organic synthesis. Due to the electronegative fluorine atoms, 1,1,2-trifluorobut-1-ene exhibits increased stability against oxidation and can participate in various reactions, including nucleophilic additions and polymerization processes. Its physical properties, such as boiling point and solubility, are affected by the fluorine substituents, which enhance its volatility compared to non-fluorinated analogs. As with many fluorinated compounds, safety precautions should be taken when handling it, as it may pose health and environmental risks.

1,1,2-trifluorobut-1-ene

383-84-6: 1,1,2-Trifluorobut-1-ene is a fluorinated organic compound characterized by its unsaturated structure, featuring a double bond between the first and second carbon atoms of a four-carbon chain. The presence of three fluorine atoms, specifically at the first and second carbon positions, significantly influences its chemical properties, making it a highly polar molecule with unique reactivity patterns. This compound is typically colorless and may have a faint odor. It is known for its applications in the synthesis of various fluorinated chemicals and as an intermediate in organic synthesis. Due to the electronegative fluorine atoms, 1,1,2-trifluorobut-1-ene exhibits increased stability against oxidation and can participate in various reactions, including nucleophilic additions and polymerization processes. Its physical properties, such as boiling point and solubility, are affected by the fluorine substituents, which enhance its volatility compared to non-fluorinated analogs. As with many fluorinated compounds, safety precautions should be taken when handling it, as it may pose health and environmental risks.

CAS 383-84-6

1,1,2-trifluorobut-1-ene

1,1,2-Trifluorobut-1-ene

Ref: 54-PC6458