Frequently Asked
Common questions about Dibenzothiophene-4-boronic acid
What is Dibenzothiophene-4-boronic acid used for?
Dibenzothiophene-4-boronic acid is a boronic acid derivative valued for its role in carbon–carbon bond-forming reactions used primarily in the pharmaceutical and medicinal chemistry industries. Key applications include suzuki–miyaura cross-coupling for biaryl and heterobiaryl synthesis and core scaffold in kinase inhibitor design for oncology therapeutics.
Where can I buy Dibenzothiophene-4-boronic acid in the USA?
ChemContract Research is a trusted USA-based supplier of Dibenzothiophene-4-boronic acid. We offer competitive pricing, fast domestic shipping from our Huntington Beach, California facility, and full quality documentation including Certificates of Analysis (CoA). Request a quote at chemistry@chem-contract.com or call +1 (714) 732-8549.
What purity levels are available for Dibenzothiophene-4-boronic acid?
ChemContract Research supplies Dibenzothiophene-4-boronic acid in multiple purity grades: ≥95% standard grade, ≥97% high-purity grade, and ≥99% ultra-high-purity grade depending on application requirements. We can also provide custom purity grades through our synthesis capabilities. Contact us for specific purity information and CoA documentation.
Can ChemContract synthesize Dibenzothiophene-4-boronic acid in custom quantities?
Yes. ChemContract Research offers custom synthesis services for Dibenzothiophene-4-boronic acid from milligram to multi-kilogram scale. Our cGMP-compliant facilities and experienced chemists can accommodate custom specifications, packaging requirements, and delivery timelines. Contact our team to discuss your project.
What drug discovery applications use Dibenzothiophene-4-boronic acid?
The Thiophene and Benzothiophene ring system(s) in Dibenzothiophene-4-boronic acid is a privileged structure in medicinal chemistry, appearing in numerous FDA-approved drugs. This scaffold is commonly used in kinase inhibitor design, GPCR modulator development, and lead optimization programs. ChemContract supplies this building block for early-stage discovery through process-scale manufacturing.
What cross-coupling reactions can I use Dibenzothiophene-4-boronic acid in?
Dibenzothiophene-4-boronic acid is primarily used in Suzuki–Miyaura cross-coupling reactions with aryl or vinyl halides under palladium catalysis. This reaction forms C–C bonds with excellent functional group tolerance and mild conditions. It can also be used in Chan–Lam coupling for C–N and C–O bond formation without transition metal catalysts under aerobic conditions.
How should I store Dibenzothiophene-4-boronic acid?
Store in a tightly sealed container at room temperature under dry conditions. Protect from prolonged moisture exposure. Store at recommended temperature in a tightly sealed container. Some heterocyclic compounds are light-sensitive. Always consult the compound-specific Safety Data Sheet (SDS) provided with your order for detailed storage requirements. ChemContract Research includes handling and storage documentation with every shipment.
What is the CAS number of Dibenzothiophene-4-boronic acid?
The CAS Registry Number for Dibenzothiophene-4-boronic acid is 108847-20-7. This unique identifier is used worldwide to reference this specific compound in chemical databases, regulatory filings, and scientific literature. ChemContract Research supplies this compound with full quality documentation. Contact us at chemistry@chem-contract.com for availability and pricing.
