Frequently Asked
Common questions about (3S,4R)-3-fluorooxan-4-amine hydrochloride
What is (3S,4R)-3-fluorooxan-4-amine hydrochloride used for?
(3S,4R)-3-fluorooxan-4-amine hydrochloride 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 metabolic blocking strategy — fluorine substitution to improve drug half-life.
Where can I buy (3S,4R)-3-fluorooxan-4-amine hydrochloride in the USA?
ChemContract Research is a trusted USA-based supplier of (3S,4R)-3-fluorooxan-4-amine hydrochloride. 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 (3S,4R)-3-fluorooxan-4-amine hydrochloride?
ChemContract Research supplies (3S,4R)-3-fluorooxan-4-amine hydrochloride 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 (3S,4R)-3-fluorooxan-4-amine hydrochloride in custom quantities?
Yes. ChemContract Research offers custom synthesis services for (3S,4R)-3-fluorooxan-4-amine hydrochloride 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.
Why is fluorine important in (3S,4R)-3-fluorooxan-4-amine hydrochloride?
The fluorine atom(s) in (3S,4R)-3-fluorooxan-4-amine hydrochloride confer several advantages in drug design: increased metabolic stability due to the strong C–F bond (485 kJ/mol), enhanced lipophilicity for improved membrane permeability, and potential for favorable electrostatic interactions with biological targets. These properties make fluorinated compounds like (3S,4R)-3-fluorooxan-4-amine hydrochloride valuable in pharmaceutical development.
What reactions can I perform with the amine group in (3S,4R)-3-fluorooxan-4-amine hydrochloride?
The amine functionality in (3S,4R)-3-fluorooxan-4-amine hydrochloride 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.
How should I store (3S,4R)-3-fluorooxan-4-amine hydrochloride?
Store in a cool, well-ventilated area away from acids and oxidizing agents. Keep containers tightly sealed as many amines are hygroscopic. Store at recommended temperature in a tightly sealed container. Protect from moisture, heat, and incompatible materials. Store at room temperature in a tightly sealed container. Protect from humidity. 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 (3S,4R)-3-fluorooxan-4-amine hydrochloride?
The CAS Registry Number for (3S,4R)-3-fluorooxan-4-amine hydrochloride is 1422188-16-6. 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.
