Product Description
Chemical Name:N,N-Dimethyl 3-boronobenzenesulfonamide
Synonyms : 3-N,N-Dimethylsulfamoylphenylboronic acid
CAS No : 871329-59-8
Purity : 98%
MolecularFormula : C8H12BNO4S
Molecular Weight:229.1
Appearance : SolidOptimized for Organic SynthesisThis compound's boronic acid functionality makes it highly effective in Suzuki-Miyaura cross-coupling reactions. Chemists rely on N,N-Dimethyl 3-boronobenzenesulfonamide for producing pharmaceutical and agrochemical intermediates, as well as for advanced research in organic synthesis. Its versatility and high purity ensure consistent and reproducible results in laboratory and industrial settings.
Safe Handling and StorageN,N-Dimethyl 3-boronobenzenesulfonamide is stable when stored in a tightly sealed, airtight container under an inert atmosphere in cool, dry conditions. Although considered non-hazardous under normal laboratory operations, direct contact with skin or eyes should be avoided. It should be stored away from moisture and strong acidic or basic environments to maintain product integrity.
FAQ's of N,N-Dimethyl 3-boronobenzenesulfonamide:
Q: How should N,N-Dimethyl 3-boronobenzenesulfonamide be stored for maximum stability?
A: Store the compound in an airtight container under an inert atmosphere, in a cool, dry location. This prevents moisture uptake and maintains stability for up to 24 months if unopened and properly stored.
Q: What are the main applications of N,N-Dimethyl 3-boronobenzenesulfonamide?
A: It is primarily used in organic synthesis, such as Suzuki-Miyaura cross-coupling reactions. Additionally, it serves as an intermediate in pharmaceutical and agrochemical production and for research purposes.
Q: When might this compound hydrolyze, and how can it be prevented?
A: Hydrolysis occurs when the compound is exposed to strong acids, bases, or moisture. To prevent degradation, always store it under inert gases and avoid contact with humid air or reactive chemicals.
Q: Where is this compound typically utilized?
A: N,N-Dimethyl 3-boronobenzenesulfonamide is utilized in research laboratories, chemical synthesis facilities, and industrial settings focused on developing pharmaceuticals, agrochemicals, and advanced organic molecules.
Q: What are the benefits of using this compound in chemical reactions?
A: Its high purity and organoboron structure enable efficient and selective cross-coupling reactions, supporting the synthesis of complex molecules with precision and reliability.
Q: Is special handling required during transport or use?
A: While not classified as dangerous goods, the compound should be transported and handled in tightly sealed containers to avoid moisture exposure and contamination. Direct skin or eye contact should be avoided.