Frequently Asked
Common questions about 3-(Aminomethyl)-2-bromothiophene 95%
What is 3-(Aminomethyl)-2-bromothiophene 95% used for?
3-(Aminomethyl)-2-bromothiophene 95% is an amine-functionalized compound with nucleophilic nitrogen reactivity used primarily in the pharmaceutical and polymer industries. Key applications include buchwald–hartwig amination for aryl c–n bond construction and grignard reagent preparation via magnesium insertion into c–br bond.
Where can I buy 3-(Aminomethyl)-2-bromothiophene 95% in the USA?
ChemContract Research is a trusted USA-based supplier of 3-(Aminomethyl)-2-bromothiophene 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 3-(Aminomethyl)-2-bromothiophene 95%?
ChemContract Research supplies 3-(Aminomethyl)-2-bromothiophene 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 3-(Aminomethyl)-2-bromothiophene 95% in custom quantities?
Yes. ChemContract Research offers custom synthesis services for 3-(Aminomethyl)-2-bromothiophene 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 reactions can I perform with the amine group in 3-(Aminomethyl)-2-bromothiophene 95%?
The amine functionality in 3-(Aminomethyl)-2-bromothiophene 95% enables diverse transformations: reductive amination with aldehydes/ketones, acylation to form amides, sulfonylation to form sulfonamides, Buchwald–Hartwig coupling with aryl halides, urea and carbamate formation, and salt generation for improved drug properties. The nucleophilicity of the nitrogen makes it one of the most versatile handles in synthetic chemistry.
What coupling reactions can I run with 3-(Aminomethyl)-2-bromothiophene 95%?
As a brominated compound, 3-(Aminomethyl)-2-bromothiophene 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.
How should I store 3-(Aminomethyl)-2-bromothiophene 95%?
Store in a cool, well-ventilated area away from acids and oxidizing agents. Keep containers tightly sealed as many amines are hygroscopic. Store at room temperature in a tightly sealed, light-resistant container. Some bromo compounds require refrigeration. 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 3-(Aminomethyl)-2-bromothiophene 95%?
The CAS Registry Number for 3-(Aminomethyl)-2-bromothiophene 95% is 157664-47-6. 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.
