Product Description
Chemical Name:4-(N,N-Diethylsulfamoyl)-2-methylphenylboronic acid
Synonyms :4-(diethylsulfamoyl)-2-methylphenyl]boronic acid
CAS No : 1217501-54-6
Purity : 98%
MolecularFormula :C11H18BNO4S
Molecular Weight:271.1
Appearance : SolidApplications in Organic SynthesisThis boronic acid derivative plays a significant role in Suzuki-Miyaura coupling, a widely-used method for forming carbon-carbon bonds in organic and pharmaceutical research. Its stability, high purity (97%), and reliable performance make it an effective building block for assembling complex molecules in R&D settings.
Safe Handling and PackagingThe compound is shipped in double PE bags, further packaged in amber glass vials or HDPE bottles to ensure chemical integrity. Though classified as non-hazardous for transport, it is imperative to handle with gloves and eye protection, adhering to standard laboratory safety protocols for chemical handling.
Storage and Shelf LifeTo guarantee optimal performance and longevity, store the product in its original, tightly sealed container, kept in a cool, dry environment away from direct light and moisture. Under these recommended conditions, it retains its properties for at least two years.
FAQ's of 4-(N,N-Diethylsulfamoyl)-2-methylphenylboronic acid:
Q: How should 4-(N,N-Diethylsulfamoyl)-2-methylphenylboronic acid be stored to maintain stability?
A: Store the compound in a tightly closed container, placed in a cool, dry area protected from light and moisture. Following these guidelines will maintain product stability for at least two years.
Q: What are the main applications of this research-grade boronic acid derivative?
A: It is primarily used as an intermediate in pharmaceutical research, and as a building block in organic synthesis, especially in Suzuki-Miyaura and other palladium-catalyzed cross-coupling reactions.
Q: When is this compound typically used in a research laboratory?
A: Researchers employ DEASMPBA during the synthesis of complex organic molecules, often as a key step in forming biaryl or arylated structures, particularly when developing novel pharmaceuticals or testing synthetic methodologies.
Q: Where can I obtain spectral data for this product?
A: 1H NMR and 13C NMR spectra for identity confirmation are available upon request from the supplier. Consult your distributor or manufacturer for these documents.
Q: What is the correct process for handling this compound in the laboratory?
A: Always wear appropriate personal protective equipment, including gloves and eye protection. Avoid ingestion and inhalation, and handle within a fume hood to minimize exposure risk.
Q: What are the benefits of using this boronic acid in cross-coupling reactions?
A: Its high purity and boronic acid functionality contribute to reliable reaction outcomes, while its stability and solubility in common organic solvents allow for consistent results in coupling processes.
Q: Is this product suitable for medicinal or food use?
A: No, this compound is intended strictly for research and development purposes and is not approved for medicinal or food-related applications.