4-Bromo-3-methoxypyridine is an organic 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 4-position and a methoxy group (-OCH3) at the 3-position contributes to its unique chemical properties. This compound typically appears as a colorless to light yellow liquid or solid, depending on its form and purity. It is soluble in organic solvents such as ethanol and dichloromethane but has limited solubility in water due to the hydrophobic nature of the bromine and methoxy substituents. 4-Bromo-3-methoxypyridine is often used in organic synthesis and medicinal chemistry, serving as an intermediate in the preparation of various pharmaceuticals and agrochemicals. Its reactivity can be attributed to the electron-withdrawing effects of the bromine atom and the electron-donating nature of the methoxy group, which can influence nucleophilic substitution reactions and other chemical transformations. Safety precautions should be observed when handling this compound, as with many halogenated organic substances.

4-Bromo-3-methoxypyridine

109911-38-8: 4-Bromo-3-methoxypyridine is an organic 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 4-position and a methoxy group (-OCH3) at the 3-position contributes to its unique chemical properties. This compound typically appears as a colorless to light yellow liquid or solid, depending on its form and purity. It is soluble in organic solvents such as ethanol and dichloromethane but has limited solubility in water due to the hydrophobic nature of the bromine and methoxy substituents. 4-Bromo-3-methoxypyridine is often used in organic synthesis and medicinal chemistry, serving as an intermediate in the preparation of various pharmaceuticals and agrochemicals. Its reactivity can be attributed to the electron-withdrawing effects of the bromine atom and the electron-donating nature of the methoxy group, which can influence nucleophilic substitution reactions and other chemical transformations. Safety precautions should be observed when handling this compound, as with many halogenated organic substances.

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CAS 109911-38-8

4-Bromo-3-methoxypyridine

4-Bromo-3-methoxypyridine

Ref: 54-OR1031532

4-Bromo-3-methoxypyridine

Ref: 10-F600471

4-Bromo-3-methoxypyridine

Ref: 3D-FB154070