Cas no 1364890-61-8 ((2R)-2-(3-fluorophenyl)pyrrolidine hydrochloride)

(2R)-2-(3-Fluorophenyl)pyrrolidine hydrochloride is a chiral pyrrolidine derivative featuring a fluorinated aromatic ring, commonly utilized as a key intermediate in pharmaceutical synthesis and medicinal chemistry research. The (R)-enantiomeric form ensures stereochemical precision, which is critical for studies involving receptor binding or enzyme inhibition. The fluorine substitution at the meta position enhances metabolic stability and modulates electronic properties, making it valuable for structure-activity relationship (SAR) investigations. The hydrochloride salt form improves solubility and handling in synthetic applications. This compound is particularly relevant in the development of CNS-targeted therapeutics and bioactive probes due to its structural versatility. High purity and well-defined stereochemistry support reproducible results in research settings.
(2R)-2-(3-fluorophenyl)pyrrolidine hydrochloride structure
1364890-61-8 structure
Product Name:(2R)-2-(3-fluorophenyl)pyrrolidine hydrochloride
CAS No:1364890-61-8
MF:C10H13ClFN
MW:201.668325185776
MDL:MFCD08751398
CID:1056326
Update Time:2025-05-24

(2R)-2-(3-fluorophenyl)pyrrolidine hydrochloride Chemical and Physical Properties

Names and Identifiers

    • (R)-2-(3-Fluorophenyl)pyrrolidine Hydrochloride
    • (2R)-2-(3-fluorophenyl)pyrrolidine hydrochloride
    • AK162214
    • AMOT0632
    • 4801AJ
    • RL01618
    • (R)-2-(3-Fluorophenyl)pyrrolidine, HCl
    • AB0049842
    • AX8262001
    • ST24035249
    • (R)-2-(3-Fluorophenyl)pyrrolidineHydrochloride
    • (R)-2-(3-FLUOROPHENYL)PYRROLIDINE HCL
    • (2R)-2-(3-Fluorophenyl)pyrrolidine--hydrogen chloride (1/1)
    • MDL: MFCD08751398
    • Inchi: 1S/C10H12FN.ClH/c11-9-4-1-3-8(7-9)10-5-2-6-12-10;/h1,3-4,7,10,12H,2,5-6H2;1H/t10-;/m1./s1
    • InChI Key: IXZAULRSYOOKSM-HNCPQSOCSA-N
    • SMILES: Cl.FC1=CC=CC(=C1)[C@H]1CCCN1

Computed Properties

  • Exact Mass: 201.07200
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 1
  • Complexity: 149
  • Topological Polar Surface Area: 12

Experimental Properties

  • PSA: 12.03000
  • LogP: 3.38100

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Additional information on (2R)-2-(3-fluorophenyl)pyrrolidine hydrochloride

Introduction to (2R)-2-(3-fluorophenyl)pyrrolidine hydrochloride (CAS No. 1364890-61-8)

(2R)-2-(3-fluorophenyl)pyrrolidine hydrochloride, identified by its CAS number 1364890-61-8, is a significant compound in the field of pharmaceutical chemistry. This compound has garnered attention due to its unique structural properties and potential applications in drug development. The presence of a fluorine atom in the phenyl ring and the pyrrolidine core makes it a promising candidate for further investigation, particularly in the design of novel therapeutic agents.

The< strong>pyrrolidine moiety is a common structural motif in many biologically active molecules, known for its ability to enhance binding affinity and metabolic stability. When combined with a< strong>3-fluorophenyl group, the compound exhibits enhanced lipophilicity and selectivity, which are critical factors in drug design. The hydrochloride salt form of this compound improves its solubility and stability, making it more suitable for various pharmaceutical applications.

Recent studies have highlighted the< strong>potential of (2R)-2-(3-fluorophenyl)pyrrolidine hydrochloride in the development of central nervous system (CNS) drugs. The fluorine atom in the phenyl ring can modulate the pharmacokinetic properties of the molecule, leading to improved blood-brain barrier penetration. This characteristic is particularly valuable in the treatment of neurological disorders where accessing the brain is a major challenge.

In addition to its CNS applications, this compound has shown promise in the treatment of< strong>inflammatory and immunomodulatory disorders. Preclinical studies have demonstrated that it can interact with various biological targets, including enzymes and receptors involved in inflammation pathways. The< strong>3-fluorophenyl group plays a crucial role in these interactions by influencing the electronic properties of the molecule, thereby enhancing its binding affinity.

The< strong>solubility enhancement provided by the hydrochloride salt form is another significant advantage of (2R)-2-(3-fluorophenyl)pyrrolidine hydrochloride. This property facilitates its formulation into various dosage forms, including oral tablets and injectable solutions. Improved solubility also contributes to better bioavailability, which is essential for achieving therapeutic efficacy.

Advances in computational chemistry have further accelerated the development of this compound. Molecular modeling studies have been instrumental in understanding its interactions with biological targets at a molecular level. These studies have provided insights into the binding mode of the< strong>pyrrolidine and< strong>3-fluorophenyl moieties, guiding the optimization of its pharmacological properties.

The< strong>pharmacokinetic profile of (2R)-2-(3-fluorophenyl)pyrrolidine hydrochloride has been extensively studied in preclinical models. Results indicate that it exhibits favorable absorption, distribution, metabolism, and excretion (ADME) properties. The compound demonstrates rapid absorption after oral administration and prolonged half-life, suggesting potential for once-daily dosing regimens.

In conclusion, (2R)-2-(3-fluorophenyl)pyrrolidine hydrochloride (CAS No. 1364890-61-8) is a versatile compound with significant potential in pharmaceutical applications. Its unique structural features, combined with favorable pharmacokinetic properties, make it an attractive candidate for further development. Ongoing research continues to explore its therapeutic applications, particularly in CNS disorders and inflammatory conditions.

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