Cas no 263564-37-0 (1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone)

1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone is a specialized organic compound featuring a thiazole core substituted with a trifluoromethylphenyl group and an ethanone moiety. Its unique structure, combining electron-withdrawing trifluoromethyl and aromatic thiazole functionalities, makes it a valuable intermediate in pharmaceutical and agrochemical synthesis. The compound exhibits high reactivity, particularly in heterocyclic transformations, enabling its use in the development of bioactive molecules. Its trifluoromethyl group enhances metabolic stability and lipophilicity, which is advantageous in drug design. The product is characterized by high purity and consistent performance, ensuring reliability in research and industrial applications. Proper handling and storage under inert conditions are recommended to maintain stability.
1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone structure
263564-37-0 structure
Product Name:1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone
CAS No:263564-37-0
MF:C12H8F3NOS
MW:271.258232116699
MDL:MFCD00278594
CID:247607
PubChem ID:2744883
Update Time:2025-11-02

1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone Chemical and Physical Properties

Names and Identifiers

    • 1-(2-[4-(TRIFLUOROMETHYL)PHENYL]-1,3-THIAZOL-4-YL)ETHAN-1-ONE
    • 1-[2-(4-Trifluoromethyl-phenyl)-thiazol-4-yl]-ethanone
    • 1-[2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-4-yl]ethanone
    • Ethanone,1-[2-[4-(trifluoromethyl)phenyl]-4-thiazolyl]-
    • 1-{2-[4-(Trifluoromethyl)phenyl]-1,3-thiazol-4-yl}ethan-1-one
    • 1-{2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-4-yl}ethanone
    • HMS566I09
    • 1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone
    • MS-22012
    • 4-Fluorophenylhydraine hydrochloride
    • FT-0644167
    • SCHEMBL15896523
    • 1-[2-[4-(trifluoromethyl)phenyl]-1, 3-thiazol-4-yl]ethanone
    • CHEBI:195114
    • MFCD00278594
    • DOKBWWZTDKYSBF-UHFFFAOYSA-N
    • DTXSID70372549
    • 263564-37-0
    • 1-(2-(4-(Trifluoromethyl)phenyl)thiazol-4-yl)ethanone
    • CCG-41615
    • CS-0357588
    • 1-(2-(4-(Trifluoromethyl)phenyl)thiazol-4-yl)ethan-1-one
    • SR-01000631676-1
    • AKOS013868266
    • SPB 03698
    • 1-[2-[4-(triluoromethyl)phenyl]-1,3-thiazol-4-yl]ethanone
    • 1-[2-[4-(TRIFLUOROMETHYL)PHENYL]-1,3-THIAZOL-4-YL]ETHAN-1-ONE
    • Maybridge1_008809
    • DB-046938
    • MDL: MFCD00278594
    • Inchi: 1S/C12H8F3NOS/c1-7(17)10-6-18-11(16-10)8-2-4-9(5-3-8)12(13,14)15/h2-6H,1H3
    • InChI Key: DOKBWWZTDKYSBF-UHFFFAOYSA-N
    • SMILES: S1C=C(C(C)=O)N=C1C1C=CC(C(F)(F)F)=CC=1

Computed Properties

  • Exact Mass: 271.02800
  • Monoisotopic Mass: 271.02786954g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 3
  • Complexity: 313
  • 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: 3.5
  • Topological Polar Surface Area: 58.2?2

Experimental Properties

  • Melting Point: 66 °C
  • PSA: 58.20000
  • LogP: 4.03150

1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone Pricemore >>

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AB227313-10 g
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AB227313-1g
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AB227313-5g
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Additional information on 1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone

Comprehensive Guide to 1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone (CAS No. 263564-37-0): Properties, Applications, and Market Insights

1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone (CAS No. 263564-37-0) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This thiazole derivative is characterized by its unique molecular structure, featuring a trifluoromethylphenyl group, which enhances its reactivity and potential applications. Researchers and industry professionals are increasingly interested in this compound due to its versatility in drug discovery and material science.

The compound's chemical stability and bioactivity make it a valuable intermediate in synthesizing novel therapeutic agents. Recent studies highlight its potential in targeting specific enzymes or receptors, aligning with the growing demand for precision medicine. Additionally, its fluorinated component contributes to improved metabolic stability, a key factor in modern drug design. These properties position 1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone as a promising candidate for further development.

In the agrochemical sector, 1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone is explored for its potential as a pesticide intermediate. The trifluoromethyl group is known to enhance the efficacy of agrochemicals, making this compound a subject of interest for sustainable farming solutions. With the global push toward environmentally friendly pesticides, this compound's role in developing low-toxicity, high-efficiency products is under investigation.

The synthesis of 1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone involves multi-step organic reactions, often starting from commercially available precursors. Optimizing its production process is a focal point for manufacturers aiming to scale up output while maintaining cost efficiency. Recent advancements in green chemistry have also influenced its synthesis, with researchers exploring catalytic methods to reduce waste and energy consumption.

Market trends indicate a rising demand for fluorinated compounds, driven by their applications in pharmaceuticals, agrochemicals, and materials science. 1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone is part of this broader trend, with its niche applications attracting investment from specialty chemical companies. Analysts project steady growth in its market value, particularly in regions with strong R&D infrastructure, such as North America, Europe, and Asia-Pacific.

From a regulatory perspective, 1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone is subject to standard chemical safety assessments. Compliance with REACH and other international regulations ensures its safe handling and transportation. Companies involved in its production must adhere to stringent quality control measures to meet industry standards and customer expectations.

In summary, 1-2-(4-Trifluoromethyl-Phenyl)-Thiazol-4-Yl-Ethanone (CAS No. 263564-37-0) represents a compelling area of research and industrial application. Its unique properties and alignment with current scientific and market trends make it a compound worth watching. As innovation continues in synthetic chemistry and applied sciences, this thiazole-based molecule is poised to play a pivotal role in future breakthroughs.

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