Cas no 1156884-70-6 (1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride)

1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride is a chemically stable, high-purity compound primarily used as a key intermediate in pharmaceutical and organic synthesis. Its dihydrochloride salt form enhances solubility and handling properties, making it suitable for precise reactions. The presence of the 4-methylimidazole moiety contributes to its reactivity in heterocyclic chemistry, particularly in the development of biologically active molecules. This compound is characterized by consistent quality, low impurity levels, and reliable performance in coupling and derivatization reactions. It is commonly employed in research settings for the synthesis of specialized ligands or pharmacophores, offering a balance of stability and reactivity for advanced chemical applications.
1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride structure
1156884-70-6 structure
Product Name:1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride
CAS No:1156884-70-6
MF:C6H11N3
MW:125.171640634537
CID:3165674
PubChem ID:43649857
Update Time:2025-06-08

1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride Chemical and Physical Properties

Names and Identifiers

    • 1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride
    • EN300-380778
    • AKOS022764490
    • ALBB-028865
    • [1-(4-methyl-1H-imidazol-2-yl)ethyl]amine dihydrochloride
    • 1-(4-methyl-1H-imidazol-2-yl)ethanamine
    • 1156884-70-6
    • 1-(4-methyl-1H-imidazol-2-yl)ethanamine dihydrochloride
    • BS-37004
    • 1-(5-methyl-1H-imidazol-2-yl)ethanamine
    • 1-(5-methyl-1H-imidazol-2-yl)ethan-1-amine
    • SCHEMBL6259613
    • MDL: MFCD12105023
    • Inchi: 1S/C6H11N3/c1-4-3-8-6(9-4)5(2)7/h3,5H,7H2,1-2H3,(H,8,9)
    • InChI Key: KLZMGVSSVJMZJW-UHFFFAOYSA-N
    • SMILES: N1C(C)=CN=C1C(C)N

Computed Properties

  • Exact Mass: 125.095
  • Monoisotopic Mass: 125.095
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 1
  • Complexity: 94.3
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 54.7A^2
  • XLogP3: -0.2

1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride Pricemore >>

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1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride Related Literature

Additional information on 1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride

Professional Introduction to 1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride (CAS No. 1156884-70-6)

1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride, a compound with the CAS number 1156884-70-6, represents a significant advancement in the field of pharmaceutical chemistry and medicinal research. This compound belongs to the class of imidazole derivatives, which have garnered considerable attention due to their diverse biological activities and potential therapeutic applications. The structural motif of this molecule, featuring a 4-methyl-1H-imidazol-2-yl substituent linked to an ethylamine group, endows it with unique chemical and pharmacological properties that make it a promising candidate for further investigation.

The dihydrochloride salt form of this compound enhances its solubility in aqueous solutions, facilitating its use in various biochemical assays and in vitro studies. This property is particularly crucial for drug development, where solubility often dictates the bioavailability and efficacy of a potential therapeutic agent. The imidazole ring in 1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride is known for its ability to interact with biological targets such as enzymes and receptors, making it a versatile scaffold for designing molecules with specific pharmacological effects.

In recent years, there has been growing interest in imidazole derivatives due to their role as intermediates in the synthesis of various pharmaceuticals. The 4-methyl-1H-imidazol-2-yl moiety is particularly noteworthy because it can be modified in multiple ways to produce analogs with tailored biological activities. For instance, studies have shown that derivatives of this type can exhibit antimicrobial, anti-inflammatory, and even anticancer properties. These findings have spurred further research into understanding the mechanisms by which these compounds exert their effects on biological systems.

The pharmaceutical industry has been actively exploring new drug candidates derived from imidazole scaffolds, recognizing their potential to address unmet medical needs. 1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride is being investigated as a precursor for more complex molecules designed to interact with specific biological pathways. Its structural features make it a valuable building block for drug discovery efforts aimed at developing novel treatments for a range of diseases.

One of the most exciting areas of research involving 1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride is its potential application in the treatment of neurological disorders. Imidazole derivatives have shown promise in modulating neurotransmitter systems, which could make them effective against conditions such as depression, anxiety, and neurodegenerative diseases. Preliminary studies suggest that this compound may interact with serotonin receptors, potentially leading to therapeutic benefits similar to those observed with selective serotonin reuptake inhibitors (SSRIs).

The synthesis of 1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride involves multi-step organic reactions that require careful optimization to ensure high yield and purity. Advanced synthetic techniques, including catalytic hydrogenation and nucleophilic substitution reactions, are employed to construct the desired molecular framework. The introduction of the hydrochloride salt form is achieved through quaternization followed by salt formation, which not only improves solubility but also enhances stability during storage and transport.

The pharmacokinetic properties of this compound are also under investigation. Understanding how 1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride is absorbed, distributed, metabolized, and excreted (ADME) is crucial for determining its suitability as a drug candidate. Preliminary pharmacokinetic studies indicate that the compound exhibits reasonable bioavailability and moderate metabolic clearance rates, suggesting that it may have a favorable pharmacokinetic profile for therapeutic use.

In conclusion, 1-(4-Methyl-1H-imidazol-2-yl)ethylamine dihydrochloride (CAS No. 1156884-70-6) represents a significant advancement in pharmaceutical chemistry with potential applications across multiple therapeutic areas. Its unique structural features and promising biological activities make it an attractive candidate for further research and development. As our understanding of its pharmacological properties continues to grow, this compound is poised to play a crucial role in the discovery and development of new treatments for human diseases.

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