Cas no 1006480-03-0 (2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol)

2-(4-Chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol is a pyrazole derivative with a hydroxyl-functionalized side chain, offering versatility as an intermediate in organic synthesis. Its structure combines a chloro-substituted pyrazole core with an ethanol moiety, enabling further functionalization for applications in pharmaceuticals, agrochemicals, or coordination chemistry. The chloro and methyl groups enhance reactivity, facilitating selective modifications, while the hydroxyl group provides a handle for derivatization or conjugation. This compound is particularly useful in the development of bioactive molecules due to its balanced lipophilicity and hydrogen-bonding capacity. High purity grades ensure consistent performance in research and industrial processes. Proper handling is advised due to potential reactivity.
2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol structure
1006480-03-0 structure
Product Name:2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol
CAS No:1006480-03-0
MF:C6H9ClN2O
MW:160.60146021843
CID:3059848
PubChem ID:19621869
Update Time:2025-11-02

2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol Chemical and Physical Properties

Names and Identifiers

    • 2-(4-Chloro-3-methyl-pyrazol-1-yl)-ethanol
    • 2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol
    • STK350074
    • 1006480-03-0
    • AKOS000312108
    • EN300-1082885
    • 2-(4-chloro-3-methylpyrazol-1-yl)ethanol
    • 2-(4-CHLORO-3-METHYL-1H-PYRAZOL-1-YL)-1-ETHANOL
    • GQB48003
    • CS-0282793
    • BBL040255
    • 2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethanol
    • MDL: MFCD06804919
    • Inchi: 1S/C6H9ClN2O/c1-5-6(7)4-9(8-5)2-3-10/h4,10H,2-3H2,1H3
    • InChI Key: WYGXZCBKSJEOHD-UHFFFAOYSA-N
    • SMILES: ClC1C(C)=NN(C=1)CCO

Computed Properties

  • Exact Mass: 160.0403406Da
  • Monoisotopic Mass: 160.0403406Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 2
  • Complexity: 112
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.5
  • Topological Polar Surface Area: 38.1?2

2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol Pricemore >>

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Additional information on 2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol

Comprehensive Overview of 2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol (CAS No. 1006480-03-0)

2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol, with the CAS number 1006480-03-0, is a specialized organic compound that has garnered significant attention in the fields of pharmaceutical research and agrochemical development. This compound belongs to the class of pyrazole derivatives, which are known for their versatile applications in medicinal chemistry and crop protection. The unique structural features of this molecule, including the chloro and methyl substituents on the pyrazole ring, contribute to its distinct chemical properties and potential biological activities.

In recent years, the demand for pyrazole-based compounds has surged due to their efficacy in drug discovery and sustainable agriculture. Researchers are particularly interested in 2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol for its potential as a building block in the synthesis of novel therapeutic agents. The compound's hydroxyl group enhances its solubility and reactivity, making it a valuable intermediate in organic synthesis. Additionally, its chloro-methyl pyrazole moiety is being explored for applications in pesticide formulations, where it may offer improved efficacy and environmental safety.

The synthesis of CAS 1006480-03-0 typically involves multi-step organic reactions, including condensation and substitution processes. Advanced analytical techniques such as NMR spectroscopy, mass spectrometry, and HPLC are employed to ensure the purity and structural integrity of the final product. Quality control is paramount, as even minor impurities can affect the compound's performance in downstream applications. This rigorous standardization aligns with the growing industry focus on high-purity intermediates for research and development.

From an environmental perspective, the biodegradability and ecological impact of pyrazole derivatives like 2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol are subjects of ongoing study. With increasing regulatory scrutiny on chemical substances, manufacturers are investing in green chemistry approaches to minimize waste and reduce hazardous byproducts. This aligns with the global trend toward sustainable chemical production, a topic frequently searched by professionals in the field.

In the pharmaceutical sector, CAS 1006480-03-0 is being investigated for its potential role in developing anti-inflammatory and antimicrobial agents. The compound's ability to modulate specific biological pathways makes it a candidate for targeted drug design. Furthermore, its structural similarity to known bioactive molecules has sparked interest in its application for central nervous system disorders, a hot topic in current medical research.

The agrochemical industry values 2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol for its potential as a precursor to next-generation crop protection products. With the rising demand for food security and sustainable farming practices, researchers are exploring how this compound could contribute to low-toxicity pesticides with minimal environmental persistence. These applications resonate with contemporary searches for eco-friendly agrochemicals and precision agriculture solutions.

From a commercial standpoint, the global market for fine chemicals like 1006480-03-0 is expanding, driven by innovation in life sciences and material science. Suppliers emphasize batch-to-batch consistency and regulatory compliance, addressing common purchaser concerns about quality assurance. The compound's patent status and manufacturing scalability are also frequently discussed topics among industry stakeholders.

In analytical applications, 2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol serves as a reference standard for method development in chromatographic analysis. Its well-characterized properties make it suitable for calibration protocols in laboratories studying similar compounds. This utility reflects the broader need for reliable analytical standards in quality control environments.

Future research directions for CAS 1006480-03-0 may explore its structure-activity relationships in greater depth, particularly how modifications to its ethanol side chain or pyrazole ring could enhance desired properties. Such investigations align with the pharmaceutical industry's focus on rational drug design and the agrochemical sector's pursuit of mode-of-action optimization.

Safety considerations for handling 2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol follow standard laboratory protocols for organic compounds, with particular attention to personal protective equipment and proper ventilation. These precautions address common workplace safety queries while ensuring compliance with chemical hygiene plans.

The storage stability of 1006480-03-0 under various conditions is another area of practical interest, with recommendations typically including cool, dry environments in airtight containers. Such storage parameters help maintain the compound's integrity over extended periods, a concern frequently raised by procurement specialists.

As regulatory frameworks evolve globally, documentation requirements for pyrazole derivatives continue to expand. Suppliers of 2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol must provide comprehensive safety data sheets and analytical certificates, addressing the due diligence needs of research institutions and industrial users alike.

In conclusion, 2-(4-chloro-3-methyl-1H-pyrazol-1-yl)ethan-1-ol (CAS 1006480-03-0) represents a versatile chemical entity with significant potential across multiple scientific disciplines. Its ongoing study reflects broader trends in molecular innovation and applied chemistry, making it a compound of enduring interest to researchers and industry professionals worldwide.

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