N-benzyl-2-hydroxyacetamide, with the CAS number 19340-77-3, is an organic compound characterized by its amide functional group and a hydroxyl group adjacent to the acetamide moiety. This compound features a benzyl group, which contributes to its hydrophobic characteristics, while the hydroxyl group enhances its solubility in polar solvents. Typically, N-benzyl-2-hydroxyacetamide exhibits moderate stability under standard conditions and can participate in various chemical reactions, including acylation and hydrolysis. Its structure allows for potential applications in pharmaceuticals, particularly as an intermediate in the synthesis of biologically active compounds. The presence of both the hydroxyl and amide functionalities may also impart specific biological activities, making it of interest in medicinal chemistry. Additionally, the compound's physical properties, such as melting point and solubility, can vary based on the purity and specific conditions under which it is handled. As with many organic compounds, proper safety measures should be observed when handling N-benzyl-2-hydroxyacetamide due to potential health hazards.

N-benzyl-2-hydroxyacetamide

19340-77-3: N-benzyl-2-hydroxyacetamide, with the CAS number 19340-77-3, is an organic compound characterized by its amide functional group and a hydroxyl group adjacent to the acetamide moiety. This compound features a benzyl group, which contributes to its hydrophobic characteristics, while the hydroxyl group enhances its solubility in polar solvents. Typically, N-benzyl-2-hydroxyacetamide exhibits moderate stability under standard conditions and can participate in various chemical reactions, including acylation and hydrolysis. Its structure allows for potential applications in pharmaceuticals, particularly as an intermediate in the synthesis of biologically active compounds. The presence of both the hydroxyl and amide functionalities may also impart specific biological activities, making it of interest in medicinal chemistry. Additionally, the compound's physical properties, such as melting point and solubility, can vary based on the purity and specific conditions under which it is handled. As with many organic compounds, proper safety measures should be observed when handling N-benzyl-2-hydroxyacetamide due to potential health hazards.

<p>N-Benzyl-2-hydroxyacetamide is a synthetic molecule that is used in the synthesis of other molecules. It is synthesized by reacting benzaldehyde with 2-aminoethanol in the presence of hydrochloric acid and sodium hydroxide. The yields are typically high, as the reaction proceeds under relatively mild conditions with few side reactions. The mechanism of this reaction is nucleophilic addition of the amino group to the carbonyl carbon atom, followed by elimination of water. N-Benzyl-2-hydroxyacetamide can be converted to various other compounds through intramolecular reactions or substitutions on its molecular structure.</p>

CAS 19340-77-3

N-benzyl-2-hydroxyacetamide

N-Benzyl-2-hydroxyacetamide

Ref: 3D-UAA34077