3-Benzylisoxazol-5-amine is an organic compound characterized by its isoxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen atoms. The presence of a benzyl group at the 3-position of the isoxazole contributes to its aromatic properties and can influence its reactivity and solubility. The amine functional group at the 5-position enhances its potential for hydrogen bonding and may play a role in biological activity. This compound is typically a solid at room temperature and may exhibit moderate to high polarity due to the functional groups present. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as compounds with isoxazole moieties are often investigated for their biological activities, including anti-inflammatory and antimicrobial properties. Additionally, the compound's specific interactions with biological targets can be influenced by the steric and electronic effects of the benzyl group, making it a subject of interest in drug design and synthesis.

3-benzylisoxazol-5-amine

119162-58-2: 3-Benzylisoxazol-5-amine is an organic compound characterized by its isoxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen atoms. The presence of a benzyl group at the 3-position of the isoxazole contributes to its aromatic properties and can influence its reactivity and solubility. The amine functional group at the 5-position enhances its potential for hydrogen bonding and may play a role in biological activity. This compound is typically a solid at room temperature and may exhibit moderate to high polarity due to the functional groups present. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as compounds with isoxazole moieties are often investigated for their biological activities, including anti-inflammatory and antimicrobial properties. Additionally, the compound's specific interactions with biological targets can be influenced by the steric and electronic effects of the benzyl group, making it a subject of interest in drug design and synthesis.

CAS 119162-58-2

3-benzylisoxazol-5-amine

3-Benzylisoxazol-5-amine

Ref: IN-DA000I9U

3-Benzyl-1,2-oxazol-5-amine

Ref: 3D-UEA16258