Product Description
Chemical Name:N,N-Dimethyl 4-boronobenzenesulfonamide
Synonyms : 4-N,N-Dimethylsulfamoylphenylboronicacid
CAS No : 486422-59-7
Purity : 95%
MolecularFormula : C8H12BNO4S
Molecular Weight:229.1
Appearance : SolidVersatile Coupling ReagentN,N-Dimethyl 4-boronobenzenesulfonamide excels as a highly selective reagent in Suzuki-Miyaura coupling, facilitating the synthesis of complex organic molecules. Its stable physical form and compatibility with multiple catalysts make it a preferred choice for research chemists seeking reliable performance in laboratory settings.
Safe and Convenient PackagingTo protect against moisture and contamination, this compound is provided in sealed plastic or glass bottles under inert atmospheric conditions. Such packaging ensures product integrity during storage and transport, crucial for maintaining high purity and activity for laboratory applications.
Storage and Shelf Life DetailsThis research-grade chemical is best stored between 2-8C in a cool, dry location, with containers tightly closed. When correctly stored, it maintains its stability and effectiveness for up to 24 months, providing flexibility and longevity for varied research schedules and synthesis workflows.
FAQ's of N,N-Dimethyl 4-boronobenzenesulfonamide:
Q: How should N,N-Dimethyl 4-boronobenzenesulfonamide be stored for optimal stability?
A: For best results, store the product at 2-8C in a tightly sealed container, protected from moisture and direct sunlight. This ensures the compound maintains purity and does not degrade over its 24-month shelf life.
Q: What are the primary uses of N,N-Dimethyl 4-boronobenzenesulfonamide in research and development?
A: The compound is mainly employed as an intermediate for organic synthesis and as a reagent in Suzuki-Miyaura coupling reactions, enabling the construction of complex organic molecules in chemical research laboratories.
Q: When is N,N-Dimethyl 4-boronobenzenesulfonamide typically utilized during synthesis?
A: It is added during the coupling stage, particularly in reactions involving organic bases or palladium catalysts, to help form carbon-carbon bonds crucial for the development of pharmaceuticals and advanced materials.
Q: Where should the product be handled to ensure safety and efficacy?
A: Handle this powder in a well-ventilated laboratory setting, using standard laboratory protective equipment, and avoid contact with moisture by working under an inert atmosphere when necessary.
Q: What process must be followed to maintain the compound's high purity?
A: After opening, immediately reseal the bottle and minimize exposure to air and moisture. Always use clean, dry tools to prevent contamination or hydrolysis, thus preserving purity and potency.
Q: How compatible is N,N-Dimethyl 4-boronobenzenesulfonamide with other chemicals used in organic synthesis?
A: It is fully compatible with various organic bases and palladium catalysts, making it suitable for a broad range of organic synthesis applications, especially for cross-coupling reactions.
Q: What benefits does using this compound offer over other similar reagents?
A: This compound offers outstanding stability under recommended storage, high purity, and safety. Its wide compatibility in catalytic systems enhances reaction efficiency, making it valuable for producing high-yield synthetic products in research environments.