2-Chloro-3-(difluoromethoxy)pyridine is a chemical compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a chlorine atom at the 2-position and a difluoromethoxy group at the 3-position contributes to its unique reactivity and properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its form and purity. It is known for its potential applications in medicinal chemistry and agrochemicals, often serving as an intermediate in the synthesis of more complex molecules. The difluoromethoxy group enhances its lipophilicity and may influence its biological activity. Additionally, the compound's structure suggests it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Safety data should be consulted, as halogenated compounds can exhibit toxicity and environmental persistence. Proper handling and storage conditions are essential to ensure safety and stability.

2-Chloro-3-(difluoromethoxy)pyridine

1206977-80-1: Pyridine, 2-chloro-3-(difluoromethoxy)-, 2-Chloro-3-(difluoromethoxy)pyridine

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CAS 1206977-80-1: 2-Chloro-3-(difluoromethoxy)pyridine

2-Chloro-3-(difluoromethoxy)pyridine

Ref: 10-F364123

2-chloro-3-(difluoromethoxy)pyridine

Ref: 3D-FC105018

2-chloro-3-(difluoroMethoxy)pyridine

Ref: IN-DA0093ZO

2-Chloro-3-(difluoromethoxy)pyridine

Ref: 54-PC421029