Cas no 1169950-70-2 (3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride)

3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride is a benzimidazole derivative with a propylamine side chain, dihydrochloride salt form. This compound is of interest in medicinal chemistry and pharmaceutical research due to its structural similarity to bioactive benzimidazole scaffolds, which are known for their diverse pharmacological properties. The dihydrochloride salt enhances solubility and stability, facilitating handling and formulation in experimental applications. Its well-defined molecular structure allows for precise modification and study of structure-activity relationships. The product is typically utilized as an intermediate in the synthesis of more complex molecules, particularly those targeting enzyme inhibition or receptor modulation. High purity and consistent quality are critical for reliable research outcomes.
3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride structure
1169950-70-2 structure
Product Name:3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride
CAS No:1169950-70-2
MF:C11H16ClN3
MW:225.717841148376
MDL:MFCD01869444
CID:3046657
PubChem ID:19195700
Update Time:2025-11-06

3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride Chemical and Physical Properties

Names and Identifiers

    • 3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-aminedihydrochloride
    • 3-(5-Methyl-1H-benzoimidazol-2-yl)-propylaminedihydrochloride
    • 3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine dihydrochloride
    • 3-(6-methyl-1H-benzimidazol-2-yl)propan-1-amine:dihydrochloride
    • 3-(6-methyl-1H-benzimidazol-2-yl)propan-1-amine;dihydrochloride
    • 3-(5-methyl-1H-1,3-benzodiazol-2-yl)propan-1-amine dihydrochloride
    • 3-(5-METHYL-1H-BENZO[D]IMIDAZOL-2-YL)PROPAN-1-AMINE DIHYDROCHLORIDE
    • AKOS005189207
    • CS-0339141
    • AT10919
    • 1169950-70-2
    • 3-(5-METHYL-1H-BENZOIMIDAZOL-2-YL)-PROPYLAMINE DIHYDROCHLORIDE
    • MFCD01869444
    • 3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride
    • MDL: MFCD01869444
    • Inchi: 1S/C11H15N3.ClH/c1-8-4-5-9-10(7-8)14-11(13-9)3-2-6-12;/h4-5,7H,2-3,6,12H2,1H3,(H,13,14);1H
    • InChI Key: AUQKZTQUUYBAIK-UHFFFAOYSA-N
    • SMILES: C(C1=NC2=CC(C)=CC=C2N1)CCN.Cl

Computed Properties

  • Exact Mass: 261.0799529g/mol
  • Monoisotopic Mass: 261.0799529g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 3
  • Complexity: 183
  • Covalently-Bonded Unit Count: 3
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 54.7?2

3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride Pricemore >>

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Additional information on 3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride

Comprehensive Overview of 3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride (CAS No. 1169950-70-2)

3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride (CAS No. 1169950-70-2) is a specialized organic compound that has garnered significant attention in pharmaceutical and biochemical research. This compound, characterized by its benzimidazole core structure, is widely studied for its potential applications in drug development and molecular biology. The dihydrochloride salt form enhances its solubility, making it a preferred choice for various experimental protocols. Researchers are particularly interested in its role as a building block for synthesizing more complex molecules, especially those targeting enzyme inhibition and receptor modulation.

The benzimidazole moiety in 3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride is a key feature that contributes to its biological activity. This structural motif is commonly found in compounds with antimicrobial, antiviral, and anticancer properties. Recent studies have explored its potential in targeted therapy, particularly in the context of personalized medicine. The compound's ability to interact with specific biological targets makes it a valuable tool for investigating signal transduction pathways and cellular responses.

In the realm of drug discovery, 3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride is often utilized as a scaffold for designing novel therapeutic agents. Its amine functionality allows for further chemical modifications, enabling researchers to tailor its properties for specific applications. For instance, it has been investigated in the development of small-molecule inhibitors for kinases and other enzymes involved in disease progression. The compound's versatility underscores its importance in modern medicinal chemistry.

Another area of interest is the compound's potential role in neuropharmacology. Preliminary studies suggest that derivatives of 3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride may interact with neurotransmitter receptors, offering insights into the treatment of neurological disorders. This aligns with the growing demand for neuroprotective agents and cognitive enhancers, topics frequently searched by both professionals and the general public. The compound's unique structure provides a foundation for exploring these avenues further.

From a synthetic perspective, the preparation of 3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride involves multi-step organic reactions, often requiring high-purity starting materials and controlled conditions. The dihydrochloride salt is typically obtained through acidification of the free base, ensuring stability and ease of handling. Researchers emphasize the importance of quality control in its synthesis, as impurities can significantly affect experimental outcomes. This aspect is particularly relevant in preclinical studies, where reproducibility is critical.

The compound's physicochemical properties, such as its melting point, solubility, and stability, are well-documented in the literature. These parameters are essential for formulating drug candidates and optimizing their delivery systems. For example, its solubility in aqueous solutions makes it suitable for in vitro assays, while its stability under various pH conditions ensures reliable performance in biological matrices. Such characteristics are frequently queried by scientists seeking to incorporate the compound into their research protocols.

In addition to its pharmaceutical applications, 3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride has been explored in material science. Its aromatic system and functional groups allow it to participate in supramolecular interactions, making it a candidate for designing advanced materials with tailored properties. This interdisciplinary potential highlights the compound's relevance beyond traditional drug development, appealing to a broader audience of researchers and innovators.

As the scientific community continues to uncover new applications for 3-(5-Methyl-1H-benzimidazol-2-yl)propan-1-amine Dihydrochloride, its demand in research laboratories and industrial settings is expected to rise. The compound's versatility, coupled with its well-characterized properties, positions it as a valuable asset in the pursuit of scientific breakthroughs. Whether in drug design, neuropharmacology, or material science, this molecule offers endless possibilities for innovation and discovery.

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