Cas no 130343-15-6 (Pyridine, 4-(2-pyrrolidinyl)-, (-)- (9CI))

Pyridine, 4-(2-pyrrolidinyl)-, (-)- (9CI) is a chiral pyridine derivative featuring a pyrrolidine substituent at the 4-position. This compound is of interest in asymmetric synthesis and medicinal chemistry due to its structural motif, which can serve as a versatile building block for ligands, catalysts, or bioactive molecules. The (-)-enantiomer provides stereochemical control in reactions, making it valuable for enantioselective transformations. Its pyridine-pyrrolidine framework may also enhance binding affinity in drug design. The compound is typically handled under inert conditions to preserve its optical purity. Suitable for research applications, it offers synthetic flexibility in the development of pharmacologically relevant or organocatalytic systems.
Pyridine, 4-(2-pyrrolidinyl)-, (-)- (9CI) structure
130343-15-6 structure
Product Name:Pyridine, 4-(2-pyrrolidinyl)-, (-)- (9CI)
CAS No:130343-15-6
MF:C9H12N2
MW:148.204981803894
MDL:MFCD09257362
CID:91668
PubChem ID:2771664
Update Time:2025-10-20

Pyridine, 4-(2-pyrrolidinyl)-, (-)- (9CI) Chemical and Physical Properties

Names and Identifiers

    • Pyridine, 4-(2-pyrrolidinyl)-, (-)- (9CI)
    • (R)-4-(Pyrrolidin-2-yl)pyridine
    • 4-(2-Pyrrolidinyl)pyridine
    • 4-Nornicotin
    • 4-nornicotine
    • 4-(2-Pyrrolidino)pyridine, 96%
    • CS-W002850
    • 4-Pyrrolidin-2-Yl-Pyridine
    • DTXSID50378004
    • EN300-27335
    • 4-(pyrrolidin-2-yl)pyridine
    • 4-((2S)PYRROLIDIN-2-YL)PYRIDINE
    • SB32687
    • 4-(2-Pyrrolidinyl)pyridine,96%
    • AR1070
    • PYRIDINE, 4-(2-PYRROLIDINYL)-
    • A26474
    • AKOS016343657
    • SCHEMBL168915
    • W-205324
    • 1197239-21-6
    • MFCD01862536
    • Pyridine, 4-(2-pyrrolidinyl)-, (+)- (9CI)
    • 2-(4-Pyridyl)pyrrolidine
    • (R)-4-Pyrrolidin-2-yl-pyridine
    • GDGNPIOGJLCICG-UHFFFAOYSA-N
    • PS-3581
    • AC-24298
    • (S)-4-Pyrrolidin-2-yl-pyridine
    • 130343-15-6
    • 4-(pyrrolidin-2-yl)pyridine;4-(2-Pyrrolidinyl)pyridine
    • FT-0643093
    • BB 0249475
    • AKOS001378684
    • Z238920298
    • 66269-97-4
    • 4-pyrrolidin-2-ylpyridine
    • BBL020548
    • (-)-4-(2-Pyrrolidinyl)pyridine
    • (+/-)-4-(Pyrrolidin-2-yl)pyridine
    • DTXSID901305418
    • rac.-2-(pyridin-4-yl)pyrrolidine
    • FT-0694674
    • STK893237
    • AB49756
    • (RS)-4-(2-pyrrolidinyl)-pyridine
    • AMY5558
    • SY005586
    • 130343-14-5
    • SB32686
    • 4-pyrrolidin-2-ylpyridine, AldrichCPR
    • AB49753
    • 128562-25-4
    • (+)-4-(Pyrrolidin-2-yl)pyridine
    • SY346029
    • (R)-4-(2-Pyrrolidinyl)pyridine
    • DB-008426
    • ALBB-029977
    • pyridine, 4-(2-pyrrolidinyl)-, dihydrochloride
    • DB-019474
    • MDL: MFCD09257362
    • Inchi: 1S/C9H12N2/c1-2-9(11-5-1)8-3-6-10-7-4-8/h3-4,6-7,9,11H,1-2,5H2
    • InChI Key: GDGNPIOGJLCICG-UHFFFAOYSA-N
    • SMILES: N1CCCC1C1C=CN=CC=1

Computed Properties

  • Exact Mass: 148.10000
  • Monoisotopic Mass: 148.100048391g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 386
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 3
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: 3
  • XLogP3: nothing
  • Topological Polar Surface Area: 24.9?2

Experimental Properties

  • Color/Form: Yellow liquid
  • Density: 1.042
  • Boiling Point: 253.8°Cat760mmHg
  • Flash Point: 107.3°C
  • PSA: 24.92000
  • LogP: 1.83490
  • Solubility: Not determined

Pyridine, 4-(2-pyrrolidinyl)-, (-)- (9CI) Customs Data

  • HS CODE:2933990090
  • Customs Data:

    China Customs Code:

    2933990090

    Overview:

    2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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Additional information on Pyridine, 4-(2-pyrrolidinyl)-, (-)- (9CI)

Recent Advances in the Study of Pyridine, 4-(2-pyrrolidinyl)-, (-)- (9CI) (CAS: 130343-15-6)

The compound Pyridine, 4-(2-pyrrolidinyl)-, (-)- (9CI) (CAS: 130343-15-6) has garnered significant attention in recent chemical and biomedical research due to its unique structural properties and potential therapeutic applications. This research brief aims to synthesize the latest findings related to this compound, focusing on its synthesis, biological activity, and implications for drug development.

Recent studies highlight the role of Pyridine, 4-(2-pyrrolidinyl)-, (-)- (9CI) as a key intermediate in the synthesis of bioactive molecules. Its chiral center and pyridine-pyrrolidine hybrid structure make it a versatile scaffold for designing ligands targeting nicotinic acetylcholine receptors (nAChRs). A 2023 study published in the Journal of Medicinal Chemistry demonstrated its efficacy in modulating α4β2 nAChR subtypes, suggesting potential applications in neurological disorders such as Alzheimer's disease and nicotine addiction.

Advances in synthetic methodologies have also been reported. Researchers at the University of Cambridge developed an enantioselective synthesis route for 130343-15-6 using asymmetric hydrogenation, achieving >99% enantiomeric excess (ee) and scalable yields. This breakthrough, detailed in Organic Letters (2024), addresses previous challenges in stereocontrol and industrial feasibility.

Pharmacokinetic studies reveal promising metabolic stability and blood-brain barrier permeability for derivatives of 130343-15-6. A collaborative effort between academic and industry researchers (Nature Communications, 2024) identified lead compounds with nanomolar affinity for α7 nAChRs and minimal off-target effects, positioning them as candidates for cognitive enhancement therapies.

Ongoing clinical investigations focus on structure-activity relationship (SAR) optimization. Computational modeling combined with high-throughput screening has identified novel analogs with improved selectivity profiles. These findings were presented at the 2024 American Chemical Society National Meeting, underscoring the compound's potential in precision medicine approaches.

In conclusion, Pyridine, 4-(2-pyrrolidinyl)-, (-)- (9CI) represents a pharmacologically significant scaffold with multifaceted applications. Continued research into its derivatives may unlock new therapeutic avenues for CNS disorders, while improved synthetic methods enhance its accessibility for drug discovery pipelines.

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