Frequently Asked
Common questions about 2-Chloro-indole-3-carbaldehyde 95%
What is 2-Chloro-indole-3-carbaldehyde 95% used for?
2-Chloro-indole-3-carbaldehyde 95% is an aldehyde with a highly electrophilic carbonyl group used primarily in the pharmaceutical and fragrance & flavor industries. Key applications include reductive amination for c–n bond formation in api synthesis and nucleophilic aromatic substitution (snar) for ether and amine formation.
Where can I buy 2-Chloro-indole-3-carbaldehyde 95% in the USA?
ChemContract Research is a trusted USA-based supplier of 2-Chloro-indole-3-carbaldehyde 95%. 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-Chloro-indole-3-carbaldehyde 95%?
ChemContract Research supplies 2-Chloro-indole-3-carbaldehyde 95% 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-Chloro-indole-3-carbaldehyde 95% in custom quantities?
Yes. ChemContract Research offers custom synthesis services for 2-Chloro-indole-3-carbaldehyde 95% 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-Chloro-indole-3-carbaldehyde 95%?
As a chlorinated compound, 2-Chloro-indole-3-carbaldehyde 95% 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-Chloro-indole-3-carbaldehyde 95%?
The Indole ring system(s) in 2-Chloro-indole-3-carbaldehyde 95% 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-Chloro-indole-3-carbaldehyde 95%?
Store at recommended temperature under inert atmosphere. Protect from air to prevent oxidation to the corresponding carboxylic acid. 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-Chloro-indole-3-carbaldehyde 95%?
The CAS Registry Number for 2-Chloro-indole-3-carbaldehyde 95% is 5059-30-3. 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.
