Cas no 1595921-61-1 (1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine)

1-(4-Methoxybutan-2-yl)-1H-pyrazol-4-amine is a pyrazole derivative featuring a methoxy-substituted butyl side chain, which enhances its solubility and reactivity in various synthetic applications. This compound serves as a versatile intermediate in pharmaceutical and agrochemical research, particularly in the development of heterocyclic compounds with potential biological activity. The presence of the 4-amine group on the pyrazole ring allows for further functionalization, making it valuable for constructing complex molecular architectures. Its structural stability and moderate polarity contribute to its utility in organic synthesis, where precise modifications are required. The compound is typically handled under controlled conditions to ensure purity and optimal performance in research applications.
1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine structure
1595921-61-1 structure
Product Name:1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine
CAS No:1595921-61-1
MF:C8H15N3O
MW:169.224201440811
CID:6192769
PubChem ID:116495821
Update Time:2025-06-09

1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine Chemical and Physical Properties

Names and Identifiers

    • 1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine
    • EN300-1108234
    • 1595921-61-1
    • SCHEMBL18494112
    • Inchi: 1S/C8H15N3O/c1-7(3-4-12-2)11-6-8(9)5-10-11/h5-7H,3-4,9H2,1-2H3
    • InChI Key: QRNHBUQDUOMIPE-UHFFFAOYSA-N
    • SMILES: O(C)CCC(C)N1C=C(C=N1)N

Computed Properties

  • Exact Mass: 169.121512110g/mol
  • Monoisotopic Mass: 169.121512110g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 4
  • Complexity: 132
  • 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
  • XLogP3: 0.1
  • Topological Polar Surface Area: 53.1?2

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Additional information on 1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine

Comprehensive Overview of 1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine (CAS No. 1595921-61-1)

1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine (CAS No. 1595921-61-1) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This compound, characterized by its unique pyrazole core and methoxybutyl side chain, is a promising intermediate for the synthesis of bioactive molecules. Researchers are increasingly exploring its potential applications due to its structural versatility and functional group compatibility. The amine moiety at the 4-position of the pyrazole ring enhances its reactivity, making it a valuable building block in drug discovery and material science.

In recent years, the demand for 1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine has surged, driven by its relevance in developing novel kinase inhibitors and antimicrobial agents. The compound's CAS No. 1595921-61-1 is frequently searched in academic and industrial databases, reflecting its growing importance. Its synthesis typically involves multi-step organic reactions, including N-alkylation and amination, which are well-documented in peer-reviewed journals. The compound's stability under physiological conditions further underscores its potential for biomedical applications.

One of the most discussed topics in the context of 1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine is its role in targeted drug delivery systems. The methoxybutyl group improves solubility, a critical factor for oral bioavailability. This aligns with current trends in personalized medicine, where researchers seek compounds with optimized pharmacokinetic profiles. Additionally, the pyrazole scaffold is known for its anti-inflammatory and antioxidant properties, making this compound a candidate for treating chronic diseases.

From an industrial perspective, CAS No. 1595921-61-1 is often associated with green chemistry initiatives. Manufacturers are exploring eco-friendly synthesis routes to minimize waste and reduce energy consumption. This resonates with the global push for sustainable chemical production, a topic frequently queried in search engines. The compound's compatibility with catalytic processes further enhances its appeal for large-scale applications.

Another area of interest is the compound's potential in crop protection. The amine functionality allows for derivatization into agrochemicals with enhanced efficacy against pests and pathogens. Given the rising focus on food security, this application is highly relevant. Researchers are also investigating its use in biodegradable polymers, leveraging its structural features to create environmentally friendly materials.

In summary, 1-(4-methoxybutan-2-yl)-1H-pyrazol-4-amine (CAS No. 1595921-61-1) is a multifaceted compound with broad applicability. Its pyrazole-amine architecture, combined with the methoxybutyl side chain, offers unparalleled opportunities in drug development, material science, and agriculture. As research progresses, this compound is poised to play a pivotal role in addressing some of the most pressing challenges in modern science.

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