2-Amino-5-methoxybenzamide, with the CAS number 1882-71-9, is an organic compound characterized by its aromatic structure, which includes an amino group (-NH2) and a methoxy group (-OCH3) attached to a benzene ring. This compound typically appears as a white to off-white solid and is soluble in polar solvents due to the presence of the amino group, which can engage in hydrogen bonding. The methoxy group contributes to its overall hydrophobic character, influencing its solubility and reactivity. 2-Amino-5-methoxybenzamide is often studied for its potential biological activities, including its role as a building block in pharmaceuticals and agrochemicals. Its chemical properties include the ability to participate in various reactions, such as acylation and amination, making it a versatile intermediate in organic synthesis. Additionally, the compound's structure allows for potential interactions with biological targets, which is of interest in medicinal chemistry. Safety data should be consulted for handling and usage, as with any chemical substance.

2-Amino-5-methoxybenzamide

1882-71-9: 2-Amino-5-(methyloxy)benzamide, 5-Methoxy-2-aminobenzamide, Benzamide, 2-Amino-5-Methoxy-, m-Anisamide, 6-amino-, 2-Amino-5-methoxybenzamide

2-Amino-5-methoxybenzamide is an aromatic compound that has been shown to induce apoptosis in human cancer cell lines. It is a directional, ring-opening reaction system that cleaves the carbon-nitrogen bond in 2-amino-5-methoxybenzamide and reacts with chloride ions to form reactive intermediates. This system was found to be effective against chlorides, as well as against myelogenous leukemia cells (K562) and colon cancer cells (HCT116). The mechanism of action of this compound is mediated by tumor cell line suppression.

CAS 1882-71-9: 2-Amino-5-methoxybenzamide

2-Amino-5-methoxybenzamide

Ref: 10-F092798

2-Amino-5-methoxybenzamide

Ref: 54-OR307692

2-Amino-5-methoxybenzamide

Ref: 3D-FA140288

Benzamide, 2-amino-5-methoxy-

Ref: IN-DA002GRO