Frequently Asked
Common questions about 3-bromopiperidine HBr >95% (NMR)
What is 3-bromopiperidine HBr >95% (NMR) used for?
3-bromopiperidine HBr >95% (NMR) is a bromo-substituted intermediate prized for its reactivity in metal-catalyzed coupling used primarily in the pharmaceutical and fine chemical industries. Key applications include grignard reagent preparation via magnesium insertion into c–br bond and cns drug scaffold (present in donepezil, methylphenidate, fentanyl class).
Where can I buy 3-bromopiperidine HBr >95% (NMR) in the USA?
ChemContract Research is a trusted USA-based supplier of 3-bromopiperidine HBr >95% (NMR). 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 3-bromopiperidine HBr >95% (NMR)?
ChemContract Research supplies 3-bromopiperidine HBr >95% (NMR) 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 3-bromopiperidine HBr >95% (NMR) in custom quantities?
Yes. ChemContract Research offers custom synthesis services for 3-bromopiperidine HBr >95% (NMR) 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 3-bromopiperidine HBr >95% (NMR)?
The Piperidine ring system(s) in 3-bromopiperidine HBr >95% (NMR) 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 coupling reactions can I run with 3-bromopiperidine HBr >95% (NMR)?
As a brominated compound, 3-bromopiperidine HBr >95% (NMR) 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.
How should I store 3-bromopiperidine HBr >95% (NMR)?
Store at room temperature in a tightly sealed, light-resistant container. Some bromo compounds require refrigeration. Store at room temperature in a well-sealed container. Some N-unsubstituted piperidines are volatile. 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 3-bromopiperidine HBr >95% (NMR)?
The CAS Registry Number for 3-bromopiperidine HBr >95% (NMR) is 102776-55-6. 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.
