N-(Phenylcarbamoyl)glycine, also known as phenylglycine or phenyl carbamoyl glycine, is an organic compound characterized by its amide functional group and the presence of both a phenyl group and a glycine moiety. It typically appears as a white to off-white crystalline solid and is soluble in polar solvents such as water and alcohols, reflecting its polar nature due to the amide bond. The compound exhibits properties typical of amino acids, including the ability to participate in hydrogen bonding, which can influence its solubility and reactivity. N-(Phenylcarbamoyl)glycine is of interest in various fields, including pharmaceuticals and biochemistry, due to its potential role as an intermediate in the synthesis of more complex molecules. Its structure allows for interactions with biological systems, making it relevant in studies of enzyme activity and protein interactions. As with many organic compounds, handling should be done with care, considering safety data and potential hazards associated with its use.

N-(phenylcarbamoyl)glycine

3016-39-5: N-(Phenylcarbamoyl)glycine, also known as phenylglycine or phenyl carbamoyl glycine, is an organic compound characterized by its amide functional group and the presence of both a phenyl group and a glycine moiety. It typically appears as a white to off-white crystalline solid and is soluble in polar solvents such as water and alcohols, reflecting its polar nature due to the amide bond. The compound exhibits properties typical of amino acids, including the ability to participate in hydrogen bonding, which can influence its solubility and reactivity. N-(Phenylcarbamoyl)glycine is of interest in various fields, including pharmaceuticals and biochemistry, due to its potential role as an intermediate in the synthesis of more complex molecules. Its structure allows for interactions with biological systems, making it relevant in studies of enzyme activity and protein interactions. As with many organic compounds, handling should be done with care, considering safety data and potential hazards associated with its use.

N-Anilinocarbonylglycine is a synthetic, optical, ethyl ester of hydantoin. It is produced by the reaction of aniline and glyoxylic acid in the presence of acetic anhydride and pyridine. The compound undergoes hydrolysis when treated with alkaline hydroxide solution. The kinetics of the reaction can be studied using a hydroxide solution as the base catalyst. In addition, N-Anilinocarbonylglycine has been shown to have membrane-stabilizing properties which may be due to its monocarboxylic acid group. This compound also undergoes catalytic deuterium isotope exchange reactions with chlorine gas in chloroform solution at room temperature.

CAS 3016-39-5

N-(phenylcarbamoyl)glycine

N-(Anilinocarbonyl)glycine

Ref: 3D-DAA01639