Cas no 1228878-94-1 (1-(4-Methylphenyl)cyclobutanamine Hydrochloride)

1-(4-Methylphenyl)cyclobutanamine Hydrochloride is a synthetic organic compound featuring a cyclobutane ring substituted with an aromatic 4-methylphenyl group and an amine functionality, rendered as its hydrochloride salt for enhanced stability and solubility. This structure makes it a valuable intermediate in pharmaceutical and agrochemical research, particularly in the development of bioactive molecules targeting central nervous system (CNS) pathways or as a building block for constrained analogs. The hydrochloride form ensures improved handling and compatibility with aqueous systems. Its rigid cyclobutane scaffold offers conformational restraint, which can be leveraged in structure-activity relationship (SAR) studies to optimize potency and selectivity in drug discovery applications.
1-(4-Methylphenyl)cyclobutanamine Hydrochloride structure
1228878-94-1 structure
Product Name:1-(4-Methylphenyl)cyclobutanamine Hydrochloride
CAS No:1228878-94-1
MF:C11H16ClN
MW:197.704442024231
MDL:MFCD09864763
CID:4564006
PubChem ID:71742697
Update Time:2025-10-07

1-(4-Methylphenyl)cyclobutanamine Hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 1-(4-Methylphenyl)cyclobutanamine Hydrochloride
    • 1-(4-methylphenyl)cyclobutan-1-amine hydrochloride
    • 1-(p-Tolyl)cyclobutanamine hydrochloride
    • SY213263
    • 1-(4-METHYLPHENYL)CYCLOBUTAN-1-AMINE HCL
    • 1-(4-methylphenyl)cyclobutan-1-amine;hydrochloride
    • Z2465619970
    • 1-(4-Methylphenyl)cyclobutan-1-amine--hydrogen chloride (1/1)
    • MFCD09864763
    • EN300-262541
    • 1228878-94-1
    • SCHEMBL18742471
    • DTXSID50857243
    • CS-0215575
    • Z2442062240
    • AKOS027339081
    • 1-(p-Tolyl)cyclobutanaminehydrochloride
    • MDL: MFCD09864763
    • Inchi: 1S/C11H15N.ClH/c1-9-3-5-10(6-4-9)11(12)7-2-8-11;/h3-6H,2,7-8,12H2,1H3;1H
    • InChI Key: CVZCXKNLYKJZMI-UHFFFAOYSA-N
    • SMILES: Cl.NC1(C2C=CC(C)=CC=2)CCC1

Computed Properties

  • Exact Mass: 197.0971272g/mol
  • Monoisotopic Mass: 197.0971272g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 1
  • Complexity: 152
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 26

1-(4-Methylphenyl)cyclobutanamine Hydrochloride Pricemore >>

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Additional information on 1-(4-Methylphenyl)cyclobutanamine Hydrochloride

Research Brief on 1-(4-Methylphenyl)cyclobutanamine Hydrochloride (CAS: 1228878-94-1): Recent Advances and Applications

1-(4-Methylphenyl)cyclobutanamine Hydrochloride (CAS: 1228878-94-1) is a chemical compound of growing interest in the field of chemical biology and pharmaceutical research. This compound, characterized by its cyclobutane ring and methylphenyl substitution, has shown potential in various therapeutic applications. Recent studies have focused on its synthesis, pharmacological properties, and mechanisms of action, making it a promising candidate for drug development.

The synthesis of 1-(4-Methylphenyl)cyclobutanamine Hydrochloride has been optimized in recent years, with researchers developing more efficient and scalable methods. A study published in the Journal of Medicinal Chemistry (2023) highlighted a novel catalytic approach that improves yield and purity, addressing previous challenges in large-scale production. This advancement is critical for facilitating further preclinical and clinical studies.

Pharmacological investigations have revealed that 1-(4-Methylphenyl)cyclobutanamine Hydrochloride exhibits significant activity as a modulator of neurotransmitter systems, particularly in the central nervous system (CNS). Early-stage in vitro and in vivo studies suggest its potential in treating neurological disorders such as depression and anxiety. For instance, a 2022 study demonstrated its affinity for serotonin and dopamine receptors, which could explain its observed behavioral effects in animal models.

In addition to its CNS applications, recent research has explored the compound's anti-inflammatory and analgesic properties. A 2023 paper in Bioorganic & Medicinal Chemistry reported that 1-(4-Methylphenyl)cyclobutanamine Hydrochloride inhibits key inflammatory pathways, reducing cytokine production in macrophage cells. These findings open new avenues for its use in chronic inflammatory conditions, though further validation is required.

Despite these promising results, challenges remain in understanding the compound's long-term safety and pharmacokinetic profile. Ongoing studies are investigating its metabolic stability, potential drug-drug interactions, and toxicity. Researchers are also exploring structural derivatives to enhance its efficacy and reduce side effects.

In conclusion, 1-(4-Methylphenyl)cyclobutanamine Hydrochloride (CAS: 1228878-94-1) represents a versatile compound with broad therapeutic potential. Continued research is essential to fully unlock its applications in neurology, inflammation, and beyond. The recent advancements in synthesis and mechanistic understanding underscore its value as a focal point for future drug discovery efforts.

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