3-Amino-4-phenylpyridine 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 3-position and a phenyl group (-C6H5) at the 4-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the amino group, which can engage in hydrogen bonding. Its structure allows for potential applications in pharmaceuticals and organic synthesis, particularly as a building block for more complex molecules. The compound may also display interesting reactivity due to the electron-donating nature of the amino group and the electron-withdrawing characteristics of the pyridine nitrogen. Additionally, it may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it valuable in synthetic organic chemistry. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken.

3-AMINO-4-PHENYLPYRIDINE

146140-99-0: 4-Phenyl-Pyridin-3-Ylamine, 4-Phenyl-3-Pyridinamine, 4-Phenylpyridin-3-Amine

3-Pyridinamine, 4-phenyl-

3-Amino-4-phenylpyridine

3-Amino-4-phenylpyridine (APY) is a cross-coupling reagent that is used to synthesize organic molecules. It can be used in the synthesis of streptonigrin, an antibiotic with broad spectrum activity against Gram-positive and Gram-negative bacteria. This compound is prepared by the electrophilic addition of 3-amino-4-phenylpyridine to a boronic acid in the presence of a base, such as lithium diisopropylamide (LDA). The lithiated reagent generated reacts with the phenylboronic acid, forming APY.

CAS 146140-99-0: 3-AMINO-4-PHENYLPYRIDINE

3-Pyridinamine, 4-phenyl-

Ref: IN-DA001DQL

3-Amino-4-phenylpyridine

Ref: 54-OR912999

3-Amino-4-phenylpyridine

Ref: 3D-FA51245

3-Amino-4-phenylpyridine

Ref: 10-F064859