The chemical substance known as {4-[(5-fluoro-2,4-dinitrophenyl)amino]-2,2,6,6-tetramethylpiperidin-1-yl}oxidanyl, with the CAS number 65870-57-7, is characterized by its complex molecular structure, which includes a piperidine ring substituted with a fluorinated dinitrophenyl group. This compound features a nitrogen atom in the piperidine ring that is bonded to an oxidanyl (hydroxyl) group, indicating its potential as a radical scavenger or antioxidant. The presence of the dinitrophenyl moiety suggests that it may exhibit significant reactivity, particularly in biological systems, where it could interact with various biomolecules. The fluorine atom enhances the lipophilicity of the molecule, potentially influencing its bioavailability and interaction with cellular membranes. Additionally, the dinitro substitution may impart unique electronic properties, making it of interest in various chemical and pharmaceutical applications. Overall, this compound's structural features suggest it may have potential uses in medicinal chemistry, particularly in the development of therapeutic agents or as a research tool in studying oxidative stress.

{4-[(5-fluoro-2,4-dinitrophenyl)amino]-2,2,6,6-tetramethylpiperidin-1-yl}oxidanyl

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N-(2,5-Dinitro-4-Fluorophenyl)-4-Amino-2,2,6,6-Tetramethylpiperidinyloxy (NDFPD) is a reactive compound that has been used for the acetylation of lysine residues on human serum albumin. It is also used as a reagent in kinetic experiments involving tyrosine and albumin. The acetylated forms of these proteins are more sensitive to hydrolysis by acid and alcohols. NDFPD reacts with primary amines to form an acylated product with an ester linkage and can be used to study enzyme reactions involving amines.

CAS 65870-57-7: {4-[(5-fluoro-2,4-dinitrophenyl)amino]-2,2,6,6-tetramethylpiperidin-1-yl}oxidanyl

N-(2,5-Dinitro-4-Fluorophenyl)-4-Amino-2,2,6,6-Tetramethylpiperidinyloxy

Ref: 3D-FD99299