Cas no 1341677-27-7 (1-(4-methoxyphenyl)-1H-pyrazol-4-ylmethanamine)

1-(4-Methoxyphenyl)-1H-pyrazol-4-ylmethanamine is a pyrazole-based amine derivative with potential applications in pharmaceutical and agrochemical research. Its structural features, including the methoxyphenyl and pyrazole moieties, make it a versatile intermediate for the synthesis of biologically active compounds. The presence of the primary amine group allows for further functionalization, enabling the development of novel derivatives with tailored properties. This compound exhibits favorable stability and solubility characteristics, facilitating its use in various synthetic pathways. Its well-defined chemical structure ensures reproducibility in research settings, making it a reliable building block for drug discovery and material science applications.
1-(4-methoxyphenyl)-1H-pyrazol-4-ylmethanamine structure
1341677-27-7 structure
Product Name:1-(4-methoxyphenyl)-1H-pyrazol-4-ylmethanamine
CAS No:1341677-27-7
MF:C11H13N3O
MW:203.240422010422
CID:5159139
PubChem ID:63173106
Update Time:2025-10-24

1-(4-methoxyphenyl)-1H-pyrazol-4-ylmethanamine Chemical and Physical Properties

Names and Identifiers

    • [1-(4-methoxyphenyl)-1H-pyrazol-4-yl]methanamine
    • 1H-Pyrazole-4-methanamine, 1-(4-methoxyphenyl)-
    • 1-(4-methoxyphenyl)-1H-pyrazol-4-ylmethanamine
    • Inchi: 1S/C11H13N3O/c1-15-11-4-2-10(3-5-11)14-8-9(6-12)7-13-14/h2-5,7-8H,6,12H2,1H3
    • InChI Key: RDCNLDRRODHCFZ-UHFFFAOYSA-N
    • SMILES: O(C)C1C=CC(=CC=1)N1C=C(C=N1)CN

Computed Properties

  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 3
  • Complexity: 192
  • XLogP3: 0.7
  • Topological Polar Surface Area: 53.1

1-(4-methoxyphenyl)-1H-pyrazol-4-ylmethanamine Pricemore >>

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Additional information on 1-(4-methoxyphenyl)-1H-pyrazol-4-ylmethanamine

Comprehensive Overview of 1-(4-Methoxyphenyl)-1H-pyrazol-4-ylmethanamine (CAS No. 1341677-27-7)

1-(4-Methoxyphenyl)-1H-pyrazol-4-ylmethanamine, with the CAS number 1341677-27-7, is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This compound belongs to the pyrazole family, a class of heterocyclic aromatic organic compounds known for their diverse biological activities. The presence of a methoxyphenyl group and an aminomethyl substituent on the pyrazole ring enhances its potential applications in drug discovery and material science.

In recent years, the demand for pyrazole derivatives has surged due to their versatility in medicinal chemistry. Researchers are particularly interested in 1-(4-Methoxyphenyl)-1H-pyrazol-4-ylmethanamine for its potential as a building block in the synthesis of novel therapeutic agents. Its structural features make it a promising candidate for targeting various biological pathways, including inflammation and central nervous system disorders. The compound's CAS no 1341677-27-7 is frequently searched in academic and industrial databases, reflecting its growing relevance.

The synthesis of 1-(4-Methoxyphenyl)-1H-pyrazol-4-ylmethanamine involves multi-step organic reactions, often starting from readily available precursors like 4-methoxyphenylhydrazine and 4-cyanopyrazole. Advanced techniques such as NMR spectroscopy and mass spectrometry are employed to confirm its purity and structural integrity. Given the increasing focus on green chemistry, researchers are also exploring eco-friendly synthetic routes to produce this compound with minimal environmental impact.

One of the most discussed topics in the context of CAS 1341677-27-7 is its potential role in drug development. The compound's ability to interact with biological targets has led to investigations into its use as a precursor for antidepressants, anticonvulsants, and even anticancer agents. Its methoxyphenyl moiety is particularly noteworthy, as it is often associated with enhanced bioavailability and metabolic stability in drug molecules. These properties make it a valuable subject for structure-activity relationship (SAR) studies.

Beyond pharmaceuticals, 1-(4-Methoxyphenyl)-1H-pyrazol-4-ylmethanamine has applications in material science. Its aromatic and heterocyclic structure lends itself to the development of organic semiconductors and light-emitting diodes (OLEDs). Researchers are exploring its use in photovoltaic cells and electronic devices, where its electron-donating and accepting capabilities could improve performance. This dual utility in both life sciences and advanced materials underscores the compound's interdisciplinary importance.

From an industrial perspective, the scalability of 1-(4-Methoxyphenyl)-1H-pyrazol-4-ylmethanamine production is a critical consideration. Manufacturers are optimizing processes to meet the rising demand while adhering to regulatory standards and safety protocols. The compound's CAS no 1341677-27-7 is often referenced in patents and technical documents, highlighting its commercial viability. Additionally, its stability under various storage conditions makes it a practical choice for large-scale applications.

In conclusion, 1-(4-Methoxyphenyl)-1H-pyrazol-4-ylmethanamine (CAS No. 1341677-27-7) is a multifaceted compound with significant potential in both scientific and industrial domains. Its unique structural attributes, coupled with its broad applicability, make it a subject of ongoing research and innovation. As the scientific community continues to uncover new uses for this compound, its importance in modern chemistry and technology is expected to grow exponentially.

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