Cas no 1015846-02-2 (1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine)

1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine is a specialized pyrazole derivative with potential applications in pharmaceutical and agrochemical research. Its unique structure, featuring an ethylpropyl substituent and a methyl group on the pyrazole ring, offers distinct reactivity and selectivity in synthetic pathways. This compound may serve as a versatile intermediate for the development of biologically active molecules, particularly in the design of enzyme inhibitors or receptor modulators. Its amine functionality provides a handle for further derivatization, enabling tailored modifications for specific research needs. The compound's stability under standard conditions ensures reliable handling in laboratory settings. Further studies are required to fully explore its synthetic utility and pharmacological properties.
1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine structure
1015846-02-2 structure
Product Name:1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine
CAS No:1015846-02-2
MF:C9H17N3
MW:167.251381635666
MDL:MFCD08457388
CID:874845
Update Time:2026-04-29

1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine Chemical and Physical Properties

Names and Identifiers

    • 4-Methyl-1-(pentan-3-yl)-1H-pyrazol-5-amine
    • 1-(1-ethylpropyl)-4-methyl-1H-pyrazol-5-amine(SALTDATA: FREE)
    • 4-methyl-2-pentan-3-ylpyrazol-3-amine
    • 1-(1-ETHYLPROPYL)-4-METHYL-1H-PYRAZOL-5-AMINE
    • AG-D-08689
    • Ambcb4022400
    • CTK3J9957
    • MolPort-004-961-653
    • CHEMBRDG-BB 4022400
    • 1H-Pyrazol-5-amine, 1-(1-ethylpropyl)-4-methyl-
    • 2-(1-ETHYL-PROPYL)-4-METHYL-2H-PYRAZOL-3-YLAMINE
    • 1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine
    • MDL: MFCD08457388
    • Inchi: InChI=1S/C9H17N3/c1-4-8(5-2)12-9(10)7(3)6-11-12/h6,8H,4-5,10H2,1-3H3
    • InChI Key: CZYXLVBBCIKKNB-UHFFFAOYSA-N
    • SMILES: CCC(CC)N1C(=C(C)C=N1)N

Computed Properties

  • Exact Mass: 167.14200
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 3

Experimental Properties

  • PSA: 43.84000
  • LogP: 2.71600

1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine Customs Data

  • HS CODE:2933199090
  • Customs Data:

    China Customs Code:

    2933199090

    Overview:

    2933199090. Other structurally non fused pyrazole ring compounds. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933199090. other compounds containing an unfused pyrazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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Additional information on 1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine

Comprehensive Overview of 1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine (CAS No. 1015846-02-2)

1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine (CAS No. 1015846-02-2) is a specialized organic compound belonging to the pyrazole class, which has garnered significant attention in pharmaceutical and agrochemical research. The compound's unique structure, featuring an ethylpropyl substituent and a methyl group on the pyrazole ring, makes it a valuable intermediate for synthesizing biologically active molecules. Researchers are particularly interested in its potential applications in drug discovery, given the rising demand for novel heterocyclic compounds with enhanced pharmacokinetic properties.

In recent years, the scientific community has focused on optimizing the synthesis of 1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine to improve yield and purity. This aligns with the broader trend of green chemistry and sustainable manufacturing, where reducing waste and energy consumption is paramount. The compound's CAS No. 1015846-02-2 is frequently searched in databases like SciFinder and Reaxys, reflecting its relevance in medicinal chemistry and material science. Its structural versatility allows for modifications that can target specific enzymes or receptors, making it a promising candidate for high-throughput screening programs.

One of the most discussed topics in relation to pyrazole derivatives is their role in addressing antibiotic resistance and chronic diseases. For instance, 1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine has been explored as a scaffold for developing anti-inflammatory agents and central nervous system (CNS) modulators. These applications are highly relevant to current healthcare challenges, such as the need for non-opioid pain relievers and neuroprotective drugs. The compound's amine functionality further enhances its ability to interact with biological targets, a feature often highlighted in computational drug design studies.

From an industrial perspective, the demand for custom synthesis of 1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine has increased, driven by its utility in preclinical research and patent filings. Companies specializing in fine chemicals often list this compound in their catalogs, catering to academic and corporate clients. Its CAS No. 1015846-02-2 serves as a critical identifier for regulatory compliance and safety documentation, ensuring seamless integration into global supply chains. Additionally, the compound's stability under various storage conditions makes it a practical choice for long-term research projects.

Emerging trends in AI-driven drug discovery have also brought 1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine into the spotlight. Machine learning algorithms frequently analyze its molecular descriptors to predict bioactivity and ADMET properties (absorption, distribution, metabolism, excretion, and toxicity). This synergy between experimental and in silico approaches accelerates the identification of lead compounds, addressing the growing need for faster and cost-effective R&D solutions. As a result, the compound is increasingly featured in open-access datasets and cheminformatics platforms.

In conclusion, 1-(1-Ethylpropyl)-4-methyl-1H-pyrazol-5-amine (CAS No. 1015846-02-2) represents a versatile and scientifically significant pyrazole derivative with broad applications in modern chemistry and life sciences. Its role in advancing drug development, sustainable synthesis, and computational modeling underscores its importance in both academic and industrial settings. As research continues to uncover new potentials for this compound, it is poised to remain a key player in the evolution of heterocyclic chemistry.

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