Frequently Asked
Common questions about Quinoline-3-boronic acid pinacolate
What is Quinoline-3-boronic acid pinacolate used for?
Quinoline-3-boronic acid pinacolate 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 Quinoline-3-boronic acid pinacolate in the USA?
ChemContract Research is a trusted USA-based supplier of Quinoline-3-boronic acid pinacolate. 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 Quinoline-3-boronic acid pinacolate?
ChemContract Research supplies Quinoline-3-boronic acid pinacolate 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 Quinoline-3-boronic acid pinacolate in custom quantities?
Yes. ChemContract Research offers custom synthesis services for Quinoline-3-boronic acid pinacolate 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 Quinoline-3-boronic acid pinacolate?
The Quinoline ring system(s) in Quinoline-3-boronic acid pinacolate 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 Quinoline-3-boronic acid pinacolate in?
Quinoline-3-boronic acid pinacolate 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 Quinoline-3-boronic acid pinacolate?
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 Quinoline-3-boronic acid pinacolate?
The CAS Registry Number for Quinoline-3-boronic acid pinacolate is 171364-85-5. 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.
