2-Amino-4-bromobenzamide is an organic compound characterized by the presence of an amino group (-NH2) and a bromine atom attached to a benzene ring, specifically at the 4-position relative to the amide functional group (-C(=O)NH2). This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols due to the presence of the amine and amide functionalities, which can engage in hydrogen bonding. The bromine substituent introduces a degree of electrophilicity and can influence the compound's reactivity, making it useful in various chemical syntheses and applications in medicinal chemistry. The presence of both the amino and amide groups suggests potential biological activity, which may be explored in drug development. Additionally, the compound's molecular structure allows for various interactions, making it a candidate for studies in pharmacology and material science. Safety data should be consulted for handling, as brominated compounds can pose health risks.

2-amino-4-bromobenzamide

2-Amino-4-bromobenzamide

2-Amino-4-bromobenzamide is a ring-opening reaction system that is used in the synthesis of isatins. It has been shown to be an efficient and rapid method for the synthesis of this class of heterocyclic compounds. The oxidative nature of this reaction makes it useful for generating reactive intermediates, which can be used for further transformations.

CAS 112253-70-0: 2-amino-4-bromobenzamide

2-Amino-4-bromobenzamide

Ref: 10-F378962

2-Amino-4-bromobenzamide

Ref: 54-OR315541

2-Amino-4-bromobenzamide

Ref: IN-DA0038Z4

2-Amino-4-bromobenzamide

Ref: 3D-MEA25370