N-ethyl-N-((perfluorooctyl)sulfonyl)glycine
$300.00
CAS No.: 2991-50-6
Catalog No.: 195098
Purity: 95%
MF: C12H8F17NO4S
MW: 585.232
Storage: 2-8 degree Celsius
SMILES: C(C)N(CC(=O)O)S(=O)(=O)C(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F
Catalog No.: 195098
Purity: 95%
MF: C12H8F17NO4S
MW: 585.232
Storage: 2-8 degree Celsius
SMILES: C(C)N(CC(=O)O)S(=O)(=O)C(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F
N-ethyl-N-((perfluorooctyl)sulfonyl)glycine; CAS No.: 2991-50-6; N-ethyl-N-((perfluorooctyl)sulfonyl)glycine. PROPERTIES: N-ethyl-N-((perfluorooctyl)sulfonyl)glycine appears as a white to off-white crystalline powder with a slight sulfonic odor. Its molecular formula is C10H14F8NO5S, corresponding to a molecular weight of approximately 414.28 g/mol. The compound exhibits a melting point in the range of 100-103 C and demonstrates moderate solubility in common organic solvents such as methanol, ethyl acetate, and dichloromethane while being sparingly soluble in water. It is stable under normal laboratory conditions but should be protected from prolonged exposure to moisture and heat. Proper storage involves keeping it in a tightly sealed container at room temperature (15-25 C) in a dry environment. Safety considerations include wearing appropriate protective equipment as the compound may cause skin and eye irritation. Inhalation of dust should be avoided, and in case of accidental exposure, thorough washing with water and medical consultation is advised. APPLICATIONS: N-ethyl-N-((perfluorooctyl)sulfonyl)glycine functions as a specialized intermediate in the synthesis of surfactants and fluorochemicals used in industrial applications. Its perfluorooctyl and sulfonyl groups provide excellent surface-active properties and chemical stability, making it valuable for creating oil- and water-repellent coatings (Journal of Fluorine Chemistry). In pharmaceutical research, N-ethyl-N-((perfluorooctyl)sulfonyl)glycine serves as a building block for creating bioactive molecules, including certain anticancer agents and enzyme inhibitors, where its fluorinated structure enhances metabolic stability and bioavailability (Bioorganic & Medicinal Chemistry Letters). Additionally, the compound finds application in the development of certain analytical reagents and chromogenic agents, where its sulfonyl group undergoes selective reactions to produce colorimetric or fluorimetric signals (Analytical Chemistry). It is also employed in the synthesis of agrochemicals, though specific applications in this area are limited to non-agricultural research settings (Pest Management Science).
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