Cas no 50534-42-4 (N,N-dimethylpyrrolidin-3-amine;dihydrochloride)

N,N-Dimethylpyrrolidin-3-amine dihydrochloride is a versatile organic compound primarily used as a building block in pharmaceutical synthesis and chemical research. Its dihydrochloride salt form enhances stability and solubility, making it suitable for various reaction conditions. The pyrrolidine scaffold is valuable in medicinal chemistry, often serving as a key intermediate for bioactive molecules, including CNS-targeting drugs. The dimethyl substitution at the amine position improves lipophilicity, facilitating membrane permeability. This compound is characterized by high purity and consistent performance, ensuring reliable results in synthetic applications. Its well-defined structure and reactivity make it a preferred choice for researchers developing novel therapeutic agents or exploring new chemical pathways.
N,N-dimethylpyrrolidin-3-amine;dihydrochloride structure
50534-42-4 structure
Product Name:N,N-dimethylpyrrolidin-3-amine;dihydrochloride
CAS No:50534-42-4
MF:C6H16Cl2N2
MW:187.110639572144
MDL:MFCD13561578
CID:858792
PubChem ID:22120278
Update Time:2025-08-04

N,N-dimethylpyrrolidin-3-amine;dihydrochloride Chemical and Physical Properties

Names and Identifiers

    • N,N-Dimethylpyrrolidin-3-amine dihydrochloride
    • 3-(Dimethylamino)pyrrolidine 2HCl
    • N,N-Dimethyl-3-pyrrolidinamine dihydrochloride
    • (S)-3-Dimethylaminopyrrolidine2HCl
    • OR52249
    • TRA0043684
    • SY002497
    • ST2407341
    • N,N-DIMETHYLPYRROLIDIN-3-AMINE 2HCL
    • AX8205022
    • W6580
    • (3S)-N,N-dimethylpyrrolidin-3-amine;dihydrochlori
    • N,N-dimethylpyrrolidin-3-amine;dihydrochloride
    • (R)-3-(Dimethylamino)pyrrolidine dihydrochloride
    • (R)-N,N-dimethylpyrrolidin-3-amine dihydrochloride
    • SB10517
    • MFCD08561117
    • DS-15615
    • DTXSID90622593
    • SY067315
    • EN300-7416205
    • MFCD13561578
    • (S)-(-)-3-Dimethylaminopyrrolidine dihydrochloride
    • (S)-(-)-3-(Dimethylamino)pyrrolidine Dihydrochloride
    • SCHEMBL8178088
    • N,N-Dimethylpyrrolidin-3-amine--hydrogen chloride (1/2)
    • MFCD08704347
    • AKOS015845292
    • (3R)-N,N-dimethylpyrrolidin-3-amine,dihydrochloride
    • 50534-42-4
    • N,N-dimethylpyrrolidin-3-aminedihydrochloride
    • SY020397
    • CS-W022911
    • DB-361247
    • MDL: MFCD13561578
    • Inchi: 1S/C6H14N2.2ClH/c1-8(2)6-3-4-7-5-6;;/h6-7H,3-5H2,1-2H3;2*1H
    • InChI Key: LCPKWRSLMCUOOZ-UHFFFAOYSA-N
    • SMILES: Cl.Cl.N1CCC(C1)N(C)C

Computed Properties

  • Exact Mass: 186.06928
  • Monoisotopic Mass: 186.0690539g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 70.9
  • Covalently-Bonded Unit Count: 3
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 15.3

Experimental Properties

  • PSA: 15.27

N,N-dimethylpyrrolidin-3-amine;dihydrochloride Security Information

N,N-dimethylpyrrolidin-3-amine;dihydrochloride Pricemore >>

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Additional information on N,N-dimethylpyrrolidin-3-amine;dihydrochloride

Recent Advances in the Study of N,N-dimethylpyrrolidin-3-amine Dihydrochloride (CAS: 50534-42-4)

N,N-dimethylpyrrolidin-3-amine dihydrochloride (CAS: 50534-42-4) is a chemical compound of significant interest in the field of chemical biology and pharmaceutical research. This compound, characterized by its pyrrolidine core and dimethylamine substitution, has been the subject of recent studies due to its potential applications in drug discovery and development. The dihydrochloride salt form enhances its solubility and stability, making it a valuable intermediate in synthetic chemistry and medicinal chemistry applications.

Recent research has focused on the synthesis and characterization of N,N-dimethylpyrrolidin-3-amine dihydrochloride, as well as its utility in the development of novel therapeutic agents. A study published in the Journal of Medicinal Chemistry (2023) demonstrated its role as a key building block in the synthesis of small-molecule inhibitors targeting G protein-coupled receptors (GPCRs). The compound's structural features, including its basic nitrogen center and rigid pyrrolidine ring, contribute to its ability to interact with biological targets, making it a versatile scaffold for drug design.

In addition to its synthetic applications, N,N-dimethylpyrrolidin-3-amine dihydrochloride has been investigated for its pharmacological properties. A preclinical study (2024) highlighted its potential as a modulator of neurotransmitter systems, particularly in the context of neurological disorders such as Parkinson's disease and schizophrenia. The compound's ability to cross the blood-brain barrier and interact with dopaminergic and serotonergic receptors underscores its therapeutic potential.

Further advancements in analytical techniques have enabled more precise characterization of N,N-dimethylpyrrolidin-3-amine dihydrochloride. High-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy have been employed to assess its purity and structural integrity, ensuring its suitability for high-throughput screening and lead optimization in drug discovery programs.

The compound's safety profile and pharmacokinetic properties have also been evaluated in recent toxicology studies. Results indicate that N,N-dimethylpyrrolidin-3-amine dihydrochloride exhibits favorable bioavailability and low toxicity, supporting its continued use in pharmaceutical research. However, further in vivo studies are needed to fully elucidate its metabolic pathways and potential side effects.

In conclusion, N,N-dimethylpyrrolidin-3-amine dihydrochloride (CAS: 50534-42-4) represents a promising compound in the field of chemical biology and drug discovery. Its structural versatility, pharmacological potential, and favorable physicochemical properties make it a valuable tool for researchers. Ongoing studies are expected to uncover new applications and optimize its use in therapeutic development.

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