N-Benzyl-2-bromobenzenesulfonamide is an organic compound characterized by its sulfonamide functional group, which is known for its biological activity, particularly in medicinal chemistry. This compound features a benzyl group attached to a sulfonamide moiety, along with a bromine atom substituted on the aromatic ring. The presence of the bromine atom enhances its reactivity and potential for further chemical modifications. N-Benzyl-2-bromobenzenesulfonamide is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific conditions. Its structure suggests potential applications in pharmaceuticals, particularly as a building block in the synthesis of biologically active molecules. The sulfonamide group can participate in various chemical reactions, making it a versatile intermediate in organic synthesis. Additionally, compounds of this nature may exhibit antimicrobial properties, which are of interest in drug development. As with many sulfonamides, safety and handling precautions should be observed due to potential toxicity and environmental impact.

N-Benzyl-2-bromobenzenesulfonamide

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N-Benzyl-2-bromobenzenesulphonamide

N-Benzyl-2-bromobenzenesulfonamide is a versatile compound with various characteristics and applications. It exhibits analgesic activity, making it suitable for pain relief purposes. Additionally, it can be used as a heterocycle in the synthesis of other compounds or as a building block in chemical reactions.

This compound has shown affinity for the adenosine A3 receptor, which plays a role in regulating inflammation and immune responses. Its interaction with this receptor suggests potential anti-inflammatory properties.

N-Benzyl-2-bromobenzenesulfonamide also possesses herbicidal properties, making it effective against unwanted plant growth. It acts by inhibiting specific enzymes involved in plant metabolism.

Furthermore, this compound has been studied for its interactions with hyaluronic acid, a key component of connective tissues. Its cationic nature allows it to form complexes with hyaluronic acid, potentially enhancing drug delivery systems or facilitating targeted therapies.

In research settings, N-Benz

CAS 321704-27-2: N-Benzyl-2-bromobenzenesulfonamide

N-Benzyl-2-bromobenzenesulfonamide

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N-Benzyl-2-bromobenzenesulphonamide

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N-Benzyl-2-bromobenzenesulfonamide

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