5-Bromo-3-(difluoromethoxy)pyridin-2-amine is a chemical compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a bromine atom at the 5-position and a difluoromethoxy group at the 3-position contributes to its unique reactivity and properties. This compound is typically used in medicinal chemistry and research due to its potential biological activity, particularly in the development of pharmaceuticals. The difluoromethoxy group enhances lipophilicity and may influence the compound's interaction with biological targets. Additionally, the presence of the amino group at the 2-position can participate in hydrogen bonding, which is crucial for its biological activity. The compound's molecular structure suggests it may exhibit interesting electronic properties and could be involved in various chemical reactions, including nucleophilic substitutions and coupling reactions. Overall, 5-bromo-3-(difluoromethoxy)pyridin-2-amine is a versatile compound with potential applications in drug discovery and development.

5-bromo-3-(difluoromethoxy)pyridin-2-amine

121936-68-3: 5-Bromo-3-(difluoromethoxy)pyridin-2-amine is a chemical compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a bromine atom at the 5-position and a difluoromethoxy group at the 3-position contributes to its unique reactivity and properties. This compound is typically used in medicinal chemistry and research due to its potential biological activity, particularly in the development of pharmaceuticals. The difluoromethoxy group enhances lipophilicity and may influence the compound's interaction with biological targets. Additionally, the presence of the amino group at the 2-position can participate in hydrogen bonding, which is crucial for its biological activity. The compound's molecular structure suggests it may exhibit interesting electronic properties and could be involved in various chemical reactions, including nucleophilic substitutions and coupling reactions. Overall, 5-bromo-3-(difluoromethoxy)pyridin-2-amine is a versatile compound with potential applications in drug discovery and development.

CAS 121936-68-3

5-bromo-3-(difluoromethoxy)pyridin-2-amine

Benzoic acid, 2-bromo-5-hydroxy-4-methoxy-

Ref: IN-DA0016G0

2-Bromo-5-hydroxy-4-methoxybenzoic acid

Ref: 54-OR470594

2-Bromo-5-hydroxy-4-methoxybenzoic acid

Ref: 10-F237359