CAS 57946-67-5

Acetamide, N-(5-amino-2-chlorophenyl)-

Description:

Acetamide, N-(5-amino-2-chlorophenyl)-, also known by its CAS number 57946-67-5, is an organic compound characterized by the presence of an acetamide functional group attached to a substituted aromatic ring. This compound features a 2-chlorophenyl moiety with an amino group at the 5-position, which contributes to its potential biological activity. It is typically a white to off-white solid, and its solubility is influenced by the presence of polar functional groups, allowing it to dissolve in polar solvents like water and alcohols. The compound may exhibit various properties such as moderate melting and boiling points, and it may participate in hydrogen bonding due to the amide group. Its structure suggests potential applications in pharmaceuticals, particularly in the development of drugs targeting specific biological pathways. As with many amides, it may also display stability under a range of conditions, although it can be sensitive to strong acids or bases. Safety data should be consulted for handling and usage guidelines.

Formula: C₈H₉ClN₂O

N-(5-Amino-2-chlorophenyl)acetamide

CAS: 57946-67-5

N-(5-Amino-2-chlorophenyl)acetamide is a molecule that has a molecular formula of C8H6ClN3. It has a molecular weight of 204.94 g/mol and it is composed of carbon, hydrogen, nitrogen, and chlorine atoms. This molecule has been shown to be an effective inhibitor for the enzyme acetylcholinesterase. N-(5-Amino-2-chlorophenyl)acetamide is structurally similar to clorgyline, which inhibits the enzyme monoamine oxidase B (MAO-B). The mechanism of inhibition by N-(5-Amino-2-chlorophenyl)acetamide is not yet fully understood, but it may be due to its ability to act as a nucleophile or its resonance stabilizing effect on the benzene ring. There are two possible geometries for this molecule: an eclipsed conformation or an anti conformation. These conformations

Formula: C₈H₉ClN₂O

Purity: Min. 95%

Molecular weight: 184.62 g/mol

Ref: 3D-HCA94667