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• Solvents and Organic Chemicals Organic Compounds Organohalogen compounds Organofluorides

Comprehensive Overview of (1R,2R)-2-Fluorocyclopentan-1-amine (CAS No. 939398-71-7)

(1R,2R)-2-Fluorocyclopentan-1-amine is a chiral fluorinated amine compound with significant potential in pharmaceutical and agrochemical applications. Its unique stereochemistry, marked by the fluorine substitution at the 2-position of the cyclopentane ring, enhances its bioactivity and selectivity. The CAS registry number 939398-71-7 ensures precise identification in chemical databases, making it a critical reference for researchers exploring small-molecule drug candidates or enantioselective synthesis.

Recent trends highlight growing interest in fluorinated building blocks like (1R,2R)-2-Fluorocyclopentan-1-amine, driven by their role in modulating pharmacokinetic properties. Searches for "chiral amines in drug discovery" or "fluorine in medicinal chemistry" reflect this demand. The compound’s stereospecificity aligns with the industry’s focus on targeted therapies, particularly in oncology and CNS disorders, where precision is paramount.

Synthetically, 939398-71-7 serves as a versatile intermediate. Its cyclopentane backbone offers rigidity, while the amine group facilitates derivatization into amides or sulfonamides. Researchers often query "how to synthesize fluorinated cyclopentanes" or "applications of chiral amines," underscoring its relevance. Green chemistry principles are also applied to its production, addressing concerns about sustainable synthesis.

In agrochemicals, (1R,2R)-2-Fluorocyclopentan-1-amine may contribute to pesticide development, leveraging fluorine’s ability to enhance ligand-receptor interactions. Queries like "fluorine in crop protection" or "chiral auxiliaries in agriculture" mirror this niche. Regulatory scrutiny on eco-friendly pesticides further elevates its appeal.

Analytical characterization of CAS 939398-71-7 involves advanced techniques like HPLC chiral separation and NMR spectroscopy, topics frequently searched alongside "amine purity analysis." Its storage typically requires inert conditions to preserve enantiomeric integrity, a detail critical for reproducibility in lab settings.

Future directions for (1R,2R)-2-Fluorocyclopentan-1-amine include exploring biocatalytic routes or AI-driven molecular design, aligning with trends like "machine learning in chemistry." Its dual utility in life sciences and materials science ensures enduring relevance, making it a staple in innovation pipelines.

• 932706-27-9((1S,2R)-2-Fluorocyclopentan-1-amine hydrochloride)
• 75198-04-8(Cyclohexanamine, 2-fluoro-, trans-)
• 79102-42-4(rac-(1R,2S)-2-fluorocyclohexan-1-amine)
• 75198-16-2(trans-2-fluorocyclohexanamine;hydrochloride)
• 1039741-13-3(2-Fluorocyclohexan-1-amine)
• 1820580-16-2((1R,2R)-2-fluorocyclohexan-1-amine hydrochloride)
• 2125943-82-8(trans-2-Fluorocyclopentan-1-amine hydrochloride)
• 1202171-77-4((1S,2S)-2-fluorocyclohexan-1-amine)
• 223756-94-3((1S,2S)-2-fluorocyclopentan-1-amine hydrochloride)
• 939426-78-5((1R,2S)-2-fluorocyclopentan-1-amine)