1,1,1-Trifluoro-4-piperidin-1-yl-but-3-en-2-one is a chemical compound characterized by its unique structure, which includes a piperidine ring and a trifluoromethyl group. The presence of the trifluoromethyl group imparts significant electronegativity and lipophilicity, influencing the compound's reactivity and interaction with biological systems. The but-3-en-2-one moiety introduces a conjugated system, which can enhance its stability and reactivity in various chemical reactions, particularly in nucleophilic additions or electrophilic substitutions. This compound may exhibit interesting pharmacological properties due to its structural features, making it a candidate for research in medicinal chemistry. Additionally, its CAS number, 215519-33-8, allows for easy identification and reference in chemical databases. As with many fluorinated compounds, it may also possess unique physical properties, such as altered boiling and melting points compared to non-fluorinated analogs. Overall, 1,1,1-trifluoro-4-piperidin-1-yl-but-3-en-2-one represents a versatile structure with potential applications in various fields, including pharmaceuticals and agrochemicals.

1,1,1-TRIFLUORO-4-PIPERIDIN-1-YL-BUT-3-EN-2-ONE

215519-33-8: 1,1,1-Trifluoro-4-piperidin-1-yl-but-3-en-2-one is a chemical compound characterized by its unique structure, which includes a piperidine ring and a trifluoromethyl group. The presence of the trifluoromethyl group imparts significant electronegativity and lipophilicity, influencing the compound's reactivity and interaction with biological systems. The but-3-en-2-one moiety introduces a conjugated system, which can enhance its stability and reactivity in various chemical reactions, particularly in nucleophilic additions or electrophilic substitutions. This compound may exhibit interesting pharmacological properties due to its structural features, making it a candidate for research in medicinal chemistry. Additionally, its CAS number, 215519-33-8, allows for easy identification and reference in chemical databases. As with many fluorinated compounds, it may also possess unique physical properties, such as altered boiling and melting points compared to non-fluorinated analogs. Overall, 1,1,1-trifluoro-4-piperidin-1-yl-but-3-en-2-one represents a versatile structure with potential applications in various fields, including pharmaceuticals and agrochemicals.

<p>1-(3-Oxo-4,4,4-trifluorobut-1-enyl)piperidine</p>

CAS 215519-33-8

1,1,1-TRIFLUORO-4-PIPERIDIN-1-YL-BUT-3-EN-2-ONE

1-(3-Oxo-4,4,4-trifluorobut-1-enyl)piperidine

Ref: 54-PC31110