2-Bromo-5-methoxybenzamide is an organic compound characterized by its aromatic structure, which includes a bromine atom and a methoxy group attached to a benzamide framework. The presence of the bromine atom at the second position and the methoxy group at the fifth position of the benzene ring contributes to its unique chemical properties, including its reactivity and solubility. This compound typically exhibits moderate polarity due to the presence of the amide functional group, which can engage in hydrogen bonding. It is often used in synthetic organic chemistry as an intermediate for the preparation of various pharmaceuticals and agrochemicals. The compound's molecular structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry. Additionally, its stability under standard conditions and the ability to undergo various chemical reactions, such as nucleophilic substitutions or coupling reactions, further enhance its utility in research and industrial applications. Safety data should be consulted for handling, as with all chemical substances, to ensure proper precautions are taken.

2-Bromo-5-methoxybenzamide

99848-43-8: 2-Bromo-5-methoxybenzamide is an organic compound characterized by its aromatic structure, which includes a bromine atom and a methoxy group attached to a benzamide framework. The presence of the bromine atom at the second position and the methoxy group at the fifth position of the benzene ring contributes to its unique chemical properties, including its reactivity and solubility. This compound typically exhibits moderate polarity due to the presence of the amide functional group, which can engage in hydrogen bonding. It is often used in synthetic organic chemistry as an intermediate for the preparation of various pharmaceuticals and agrochemicals. The compound's molecular structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry. Additionally, its stability under standard conditions and the ability to undergo various chemical reactions, such as nucleophilic substitutions or coupling reactions, further enhance its utility in research and industrial applications. Safety data should be consulted for handling, as with all chemical substances, to ensure proper precautions are taken.

CAS 99848-43-8

2-Bromo-5-methoxybenzamide

2-Bromo-5-methoxybenzamide

Ref: 54-OR1005802

2-Bromo-5-methoxybenzamide

Ref: 10-F713768

2-bromo-5-methoxybenzamide

Ref: 3D-ZDA84843