4-Amino-3-fluoropyridine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of an amino group (-NH2) at the 4-position and a fluorine atom at the 3-position of the pyridine ring defines its structure and reactivity. This compound is typically a colorless to pale yellow solid and is soluble in polar solvents such as water and alcohols. It exhibits basic properties due to the amino group, allowing it to participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. 4-Amino-3-fluoropyridine is of interest in medicinal chemistry and materials science, often serving as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its fluorine substituent can enhance biological activity and influence the compound's physicochemical properties. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure.

4-Amino-3-Fluoropyridine

4-Amino-3-fluoropyridine

4-Amino-3-fluoropyridine (4AFP) is an analog of the nucleophilic guanidine compound, which has been shown to be effective in the treatment of multiple sclerosis. The uptake and pharmacokinetic properties of 4AFP were studied in humans and found to be similar to those of the parent compound, 3-amino-2,6-difluoropyridine. 4AFP was also found to be effective in a clinical trial for chronic progressive multiple sclerosis. The demyelinating effects of 4AFP are due to its ability to inhibit myelin basic protein synthesis.

CAS 2247-88-3: 4-Amino-3-Fluoropyridine

4-Amino-3-fluoropyridine

Ref: IN-DA003KPI

4-Amino-3-fluoropyridine

Ref: 3B-A2383

4-Amino-3-fluoropyridine

Ref: 3D-FA08161

4-Amino-3-fluoropyridine

Ref: 54-PC1163

4-Amino-3-fluoropyridine

Ref: 10-F045062