Frequently Asked
Common questions about 2,3-Dichloro-4-pyridineboronic acid
What is 2,3-Dichloro-4-pyridineboronic acid used for?
2,3-Dichloro-4-pyridineboronic 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 nucleophilic aromatic substitution (snar) for ether and amine formation.
Where can I buy 2,3-Dichloro-4-pyridineboronic acid in the USA?
ChemContract Research is a trusted USA-based supplier of 2,3-Dichloro-4-pyridineboronic 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 2,3-Dichloro-4-pyridineboronic acid?
ChemContract Research supplies 2,3-Dichloro-4-pyridineboronic 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 2,3-Dichloro-4-pyridineboronic acid in custom quantities?
Yes. ChemContract Research offers custom synthesis services for 2,3-Dichloro-4-pyridineboronic 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 coupling reactions can I run with 2,3-Dichloro-4-pyridineboronic acid?
As a chlorinated compound, 2,3-Dichloro-4-pyridineboronic acid is an excellent substrate for palladium-catalyzed cross-coupling reactions including Suzuki, Heck, Negishi, Sonogashira, and Buchwald–Hartwig amination. It can also be used for Grignard reagent preparation, metal–halogen exchange with organolithium reagents, and nucleophilic substitution reactions.
What drug discovery applications use 2,3-Dichloro-4-pyridineboronic acid?
The Pyridine ring system(s) in 2,3-Dichloro-4-pyridineboronic 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.
How should I store 2,3-Dichloro-4-pyridineboronic acid?
Store in a tightly sealed container at room temperature under dry conditions. Protect from prolonged moisture exposure. Store at recommended temperature in a well-sealed container. Protect from moisture and strong bases. 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 2,3-Dichloro-4-pyridineboronic acid?
The CAS Registry Number for 2,3-Dichloro-4-pyridineboronic acid is 951677-39-7. 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.
