Cas no 160241-65-6 (2-(2-Methylthiazol-4-yl)phenol)

2-(2-Methylthiazol-4-yl)phenol is a heterocyclic compound featuring a phenol moiety linked to a 2-methylthiazole ring. This structure imparts unique chemical properties, making it valuable in pharmaceutical and agrochemical research. The thiazole component enhances its potential as a building block for bioactive molecules, particularly in the development of antimicrobial and anti-inflammatory agents. Its phenolic group allows for further functionalization, enabling tailored modifications for specific applications. The compound exhibits stability under standard conditions, ensuring reliable performance in synthetic workflows. Its well-defined structure and reactivity profile make it a useful intermediate in organic synthesis, particularly for constructing complex heterocyclic systems.
2-(2-Methylthiazol-4-yl)phenol structure
160241-65-6 structure
Product Name:2-(2-Methylthiazol-4-yl)phenol
CAS No:160241-65-6
MF:C10H9NOS
MW:191.249561071396
MDL:MFCD00665949
CID:91989
PubChem ID:18801453
Update Time:2025-11-02

2-(2-Methylthiazol-4-yl)phenol Chemical and Physical Properties

Names and Identifiers

    • 2-(2-Methylthiazol-4-yl)phenol
    • BUTTPARK 16\06-63
    • 2-(2-Methyl-4-thiazolyl)phenol
    • 2-(2-methyl-1,3-thiazol-4-yl)phenol
    • 2-(1-METHYL-1 H-TETRAZOL-5-YLSULFANYL)-ETHYLAMINE
    • 2-(2-METHYL-THIAZOL-4-YL)-PHENOL
    • 2,6-Dioxo-1,2,3,6-Tetrahydro-4-Pyrimidinecarbaldehyde
    • AKOS002663680
    • Phenol, 2-(2-methyl-4-thiazolyl)-
    • MFCD00665949
    • EN300-110475
    • AS-61579
    • 160241-65-6
    • DTXSID70596384
    • A883228
    • F74380
    • SCHEMBL1093303
    • Z1201620447
    • DB-103494
    • MDL: MFCD00665949
    • Inchi: 1S/C10H9NOS/c1-7-11-9(6-13-7)8-4-2-3-5-10(8)12/h2-6,12H,1H3
    • InChI Key: LYLPLPWQCLBGHW-UHFFFAOYSA-N
    • SMILES: S1C(C)=NC(=C1)C1C=CC=CC=1O

Computed Properties

  • Exact Mass: 140.02200
  • Monoisotopic Mass: 191.04048508g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 1
  • Complexity: 176
  • 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
  • Surface Charge: 0
  • Tautomer Count: 3
  • XLogP3: 2.7
  • Topological Polar Surface Area: 61.4?2

Experimental Properties

  • Color/Form: Brown or white powder
  • Density: 1.257
  • Melting Point: 61-64℃
  • Boiling Point: 331.2°Cat760mmHg
  • Flash Point: 154.1°C
  • Refractive Index: 1.629
  • PSA: 82.79000
  • LogP: -1.12430
  • Solubility: Not determined

2-(2-Methylthiazol-4-yl)phenol Security Information

  • Hazard Category Code: 22
  • Safety Instruction: S26-S36/37/39-S45
  • Hazardous Material Identification: C Xi
  • Risk Phrases:R34

2-(2-Methylthiazol-4-yl)phenol Customs Data

  • HS CODE:2934100090
  • Customs Data:

    China Customs Code:

    2934100090

    Overview:

    2934100090. Compounds that structurally contain a non fused thiazole ring(Whether hydrogenated or not). VAT:17.0%. Tax refund rate:9.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2934100090 other compounds containing an unfused thiazole ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

2-(2-Methylthiazol-4-yl)phenol Pricemore >>

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SHANG HAI XIAN DING Biotechnology Co., Ltd.
F-QR276-250mg
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abcr
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2-(2-Methyl-4-thiazolyl)phenol; 97%
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Additional information on 2-(2-Methylthiazol-4-yl)phenol

Comprehensive Guide to 2-(2-Methylthiazol-4-yl)phenol (CAS No. 160241-65-6): Properties, Applications, and Market Insights

2-(2-Methylthiazol-4-yl)phenol (CAS No. 160241-65-6) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This heterocyclic phenol derivative, featuring a methylthiazole moiety, exhibits unique chemical properties that make it valuable for various industrial and scientific applications. With the growing demand for thiazole-based compounds in drug discovery, this molecule has become a subject of interest for researchers exploring novel bioactive molecules.

The molecular structure of 2-(2-Methylthiazol-4-yl)phenol combines aromatic and heterocyclic characteristics, offering diverse reactivity patterns. Its phenolic hydroxyl group provides sites for further chemical modifications, while the methylthiazole ring contributes to its potential biological activity. Recent studies have highlighted its role as a building block for more complex molecules, particularly in the development of antimicrobial agents and enzyme inhibitors, addressing current concerns about antibiotic resistance and targeted therapies.

In pharmaceutical applications, 2-(2-Methylthiazol-4-yl)phenol serves as a crucial intermediate in synthesizing potential drug candidates. Its structural features align with current trends in fragment-based drug design, where small molecular fragments are optimized into lead compounds. The compound's ability to interact with biological targets makes it particularly relevant for research into neurological disorders and metabolic diseases, topics that dominate current medical research queries in scientific databases.

The agrochemical industry has shown increasing interest in thiazole-containing compounds like 2-(2-Methylthiazol-4-yl)phenol due to their potential as plant growth regulators and pest control agents. As sustainable agriculture becomes a global priority, researchers are investigating this compound's derivatives for their environmental compatibility and targeted action against agricultural pathogens, addressing the growing market demand for eco-friendly crop protection solutions.

From a synthetic chemistry perspective, 2-(2-Methylthiazol-4-yl)phenol presents interesting challenges and opportunities. Its preparation typically involves heterocyclic condensation reactions, with recent advances focusing on green chemistry approaches to improve yield and reduce waste. These methodologies align with the pharmaceutical industry's shift toward sustainable synthesis, a topic frequently searched by chemistry professionals and environmental researchers.

Analytical characterization of 2-(2-Methylthiazol-4-yl)phenol employs advanced techniques such as HPLC-MS and NMR spectroscopy, reflecting the compound's complexity. Quality control protocols for this material emphasize purity standards crucial for research applications, particularly in high-throughput screening systems where compound integrity directly affects experimental outcomes. These aspects are critical for laboratories sourcing this chemical for their investigations.

The commercial availability of 2-(2-Methylthiazol-4-yl)phenol has expanded in recent years, with suppliers offering various quantities to meet research demands. Market analysis indicates growing procurement of this compound by contract research organizations and academic institutions, particularly those focusing on medicinal chemistry and chemical biology programs. Pricing trends reflect its status as a specialty chemical with significant research value.

Storage and handling of 2-(2-Methylthiazol-4-yl)phenol require standard laboratory precautions for organic compounds. While not classified as hazardous under normal conditions, proper chemical storage protocols should be followed to maintain stability. The compound's shelf life and stability data are important considerations for research facilities, especially those engaged in long-term studies requiring consistent material quality.

Future research directions for 2-(2-Methylthiazol-4-yl)phenol include exploring its potential in material science applications, particularly in developing functional polymers and coordination complexes. The compound's molecular architecture suggests possible utility in creating advanced materials with specific optical or electronic properties, an area gaining traction in materials science queries and publications.

In conclusion, 2-(2-Methylthiazol-4-yl)phenol (CAS No. 160241-65-6) represents a versatile chemical entity with broad potential across multiple scientific disciplines. Its unique structural features and reactivity profile continue to inspire innovative applications in pharmaceutical development, agricultural science, and advanced materials research. As scientific understanding of heterocyclic compounds deepens, this molecule is poised to remain relevant in addressing contemporary challenges in health, agriculture, and technology.

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