The chemical substance known as (2,3,4,5,6-pentafluorophenyl) 3-(1,3-dioxolan-2-yl)thiophene-2-carboxylate, with the CAS number 910037-02-4, is a complex organic compound characterized by its unique structural features. It contains a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur, and is substituted with a carboxylate group, enhancing its reactivity and potential applications in organic synthesis. The presence of a 1,3-dioxolane moiety contributes to its stability and solubility in various solvents. The pentafluorophenyl group significantly influences the compound's electronic properties, making it highly electron-deficient, which can enhance its interactions in various chemical environments. This compound may exhibit interesting optical and electronic properties, making it a candidate for applications in materials science, particularly in organic electronics and photonic devices. Its fluorinated nature can also impart unique characteristics such as increased lipophilicity and altered reactivity, which are valuable in medicinal chemistry and agrochemical applications. Overall, this compound represents a versatile building block in advanced organic synthesis.

(2,3,4,5,6-pentafluorophenyl) 3-(1,3-dioxolan-2-yl)thiophene-2-carboxylate

910037-02-4: The chemical substance known as (2,3,4,5,6-pentafluorophenyl) 3-(1,3-dioxolan-2-yl)thiophene-2-carboxylate, with the CAS number 910037-02-4, is a complex organic compound characterized by its unique structural features. It contains a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur, and is substituted with a carboxylate group, enhancing its reactivity and potential applications in organic synthesis. The presence of a 1,3-dioxolane moiety contributes to its stability and solubility in various solvents. The pentafluorophenyl group significantly influences the compound's electronic properties, making it highly electron-deficient, which can enhance its interactions in various chemical environments. This compound may exhibit interesting optical and electronic properties, making it a candidate for applications in materials science, particularly in organic electronics and photonic devices. Its fluorinated nature can also impart unique characteristics such as increased lipophilicity and altered reactivity, which are valuable in medicinal chemistry and agrochemical applications. Overall, this compound represents a versatile building block in advanced organic synthesis.

CAS 910037-02-4

(2,3,4,5,6-pentafluorophenyl) 3-(1,3-dioxolan-2-yl)thiophene-2-carboxylate

Perfluorophenyl 3-(1,3-dioxolan-2-yl)thiophene-2-carboxylate

Ref: 10-F779165

Pentafluorophenyl 3-(1,3-dioxolan-2-yl)thiophene-2-carboxylate

Ref: 54-PC8540