2-Fluoronicotinic acid methyl ester is an organic compound characterized by its pyridine ring structure, which features a fluorine atom at the 2-position and a methyl ester functional group. This compound is a derivative of nicotinic acid, where the carboxylic acid group is esterified with methanol. It typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the fluorine atom can influence its reactivity and polarity, making it useful in various chemical syntheses and pharmaceutical applications. 2-Fluoronicotinic acid methyl ester may exhibit biological activity, potentially serving as a building block in the development of agrochemicals or pharmaceuticals. Its solubility in organic solvents and moderate stability under standard conditions make it a versatile compound in synthetic organic chemistry. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

2-Fluoronicotinic acid methyl ester

446-26-4: 3-Pyridinecarboxylic Acid, 2-Fluoro-, Methyl Ester, Methyl 2-fluoronicotinate, Methyl 2-Fluoropyridine-3-Carboxylate, Methyl 2-Fluoro-3-Pyridinecarboxylate

Methyl 2-Fluoronicotinate

Methyl 2-fluoropyridine-3-carboxylate is an integrase inhibitor that binds to the active site of HIV integrase and blocks the integration of viral DNA into host cells. Methyl 2-fluoropyridine-3-carboxylate has been shown to be a potent antiviral against HIV type 1 and HIV type 2. It has also been shown to inhibit the replication of other viruses, such as herpes simplex virus type 1 and influenza A virus. This compound also has anti-inflammatory effects in a mouse model of colitis.

CAS 446-26-4: 2-Fluoronicotinic acid methyl ester

Methyl 2-Fluoronicotinate

Ref: 10-F066892

Methyl 2-fluoropyridine-3-carboxylate

Ref: 3D-FM104639

Methyl 2-fluoronicotinate

Ref: 54-PC201254

Methyl 2-fluoropyridine-3-carboxylate

Ref: FT-F13032

Methyl 2-fluoronicotinate

Ref: IN-DA00I8G1