Cas no 1609407-55-7 ((1-ethyl-3-methyl-pyrazol-4-yl)methanamine;dihydrochloride)

(1-Ethyl-3-methyl-pyrazol-4-yl)methanamine dihydrochloride is a pyrazole-derived amine compound with significant utility in pharmaceutical and chemical synthesis. Its dihydrochloride salt form enhances stability and solubility, making it suitable for precise applications in medicinal chemistry and drug development. The ethyl and methyl substituents on the pyrazole ring contribute to its structural versatility, enabling its use as a key intermediate in the synthesis of bioactive molecules. The compound’s well-defined crystalline structure ensures consistent purity and reactivity, critical for research and industrial processes. Its compatibility with various reaction conditions further underscores its value as a reliable building block in heterocyclic chemistry.
(1-ethyl-3-methyl-pyrazol-4-yl)methanamine;dihydrochloride structure
1609407-55-7 structure
Product Name:(1-ethyl-3-methyl-pyrazol-4-yl)methanamine;dihydrochloride
CAS No:1609407-55-7
MF:C7H14ClN3
MW:175.659160137177
MDL:MFCD26959751
CID:4608773
Update Time:2025-10-31

(1-ethyl-3-methyl-pyrazol-4-yl)methanamine;dihydrochloride Chemical and Physical Properties

Names and Identifiers

    • [(1-ethyl-3-methyl-1H-pyrazol-4-yl)methyl]amine dihydrochloride
    • (1-ethyl-3-methyl-pyrazol-4-yl)methanamine;dihydrochloride
    • MDL: MFCD26959751
    • Inchi: 1S/C7H13N3.ClH/c1-3-10-5-7(4-8)6(2)9-10;/h5H,3-4,8H2,1-2H3;1H
    • InChI Key: VXOMXPJBWORTCO-UHFFFAOYSA-N
    • SMILES: C(C1=CN(CC)N=C1C)N.Cl

Computed Properties

  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2

(1-ethyl-3-methyl-pyrazol-4-yl)methanamine;dihydrochloride Pricemore >>

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Additional information on (1-ethyl-3-methyl-pyrazol-4-yl)methanamine;dihydrochloride

Recent Advances in the Study of (1-ethyl-3-methyl-pyrazol-4-yl)methanamine Dihydrochloride (CAS: 1609407-55-7)

The compound (1-ethyl-3-methyl-pyrazol-4-yl)methanamine dihydrochloride (CAS: 1609407-55-7) has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This small molecule, characterized by its pyrazole core and amine functionality, has shown promising potential in various therapeutic applications, particularly in the modulation of protein-protein interactions and enzyme inhibition. Recent studies have focused on its synthesis, structural optimization, and biological evaluation, aiming to elucidate its mechanism of action and therapeutic efficacy.

One of the key findings in recent literature is the role of (1-ethyl-3-methyl-pyrazol-4-yl)methanamine dihydrochloride as a selective inhibitor of certain kinases involved in inflammatory and oncogenic pathways. Researchers have demonstrated its ability to bind with high affinity to specific kinase domains, thereby disrupting downstream signaling cascades. This property makes it a valuable candidate for the development of targeted therapies for diseases such as cancer and autoimmune disorders. Structural-activity relationship (SAR) studies have further refined the compound's scaffold to enhance its potency and selectivity.

In addition to its kinase inhibitory activity, (1-ethyl-3-methyl-pyrazol-4-yl)methanamine dihydrochloride has been investigated for its potential as a building block in the synthesis of more complex pharmacophores. Its amine group serves as a versatile handle for further chemical modifications, enabling the creation of derivatives with improved pharmacokinetic properties. Recent synthetic methodologies have focused on optimizing the yield and purity of this compound, ensuring its suitability for large-scale production and preclinical testing.

Another area of interest is the compound's application in drug discovery pipelines. High-throughput screening (HTS) campaigns have identified (1-ethyl-3-methyl-pyrazol-4-yl)methanamine dihydrochloride as a hit molecule for several targets, including G protein-coupled receptors (GPCRs) and ion channels. These findings have spurred further investigations into its therapeutic potential, with some studies reporting promising in vitro and in vivo results. For instance, animal models of neuropathic pain have shown significant alleviation of symptoms upon administration of this compound, suggesting its utility in pain management.

Despite these advancements, challenges remain in the development of (1-ethyl-3-methyl-pyrazol-4-yl)methanamine dihydrochloride as a therapeutic agent. Issues such as bioavailability, metabolic stability, and off-target effects need to be addressed through rigorous preclinical studies. Recent efforts have focused on formulating the compound in various delivery systems, including nanoparticles and liposomes, to enhance its therapeutic index. Additionally, computational modeling and molecular dynamics simulations are being employed to predict its behavior in biological systems and guide further optimization.

In conclusion, (1-ethyl-3-methyl-pyrazol-4-yl)methanamine dihydrochloride (CAS: 1609407-55-7) represents a promising scaffold in chemical biology and drug discovery. Its diverse biological activities and synthetic versatility make it a valuable tool for researchers aiming to develop novel therapeutics. Future studies should focus on translating these findings into clinical applications, addressing the aforementioned challenges, and exploring its potential in combination therapies. The ongoing research underscores the importance of this compound in advancing our understanding of disease mechanisms and therapeutic interventions.

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