Cas no 1826-17-1 (4-Methyl-2-phenylthiazole)

4-Methyl-2-phenylthiazole is a heterocyclic organic compound featuring a thiazole core substituted with a methyl group at the 4-position and a phenyl ring at the 2-position. This structure imparts notable stability and versatility, making it valuable in pharmaceutical and agrochemical research. Its electron-rich aromatic system facilitates applications as a building block in medicinal chemistry, particularly in the synthesis of bioactive molecules. The compound exhibits favorable physicochemical properties, including moderate solubility in organic solvents and thermal stability, enhancing its utility in synthetic workflows. Its well-defined reactivity profile allows for selective functionalization, supporting its role in the development of novel thiazole-based derivatives.
4-Methyl-2-phenylthiazole structure
4-Methyl-2-phenylthiazole structure
Product Name:4-Methyl-2-phenylthiazole
CAS No:1826-17-1
MF:C10H9NS
MW:175.250160932541
MDL:MFCD00272328
CID:83968
PubChem ID:551876
Update Time:2025-06-08

4-Methyl-2-phenylthiazole Chemical and Physical Properties

Names and Identifiers

    • 4-Methyl-2-phenylthiazole
    • 4-Methyl-2-phenyl-thiazole
    • 2-phenyl-4-methyl-1,3-thiazole
    • 2-phenyl-4-methylthiazole
    • 4-Methyl-2-phenyl-thiazol
    • Thiazole,4-methyl-2-phenyl
    • 4-Methyl-2-phenyl-1,3-thiazole
    • 4-Methyl-2-phenyl-1,3-thiazole #
    • FT-0748156
    • ?4-METHYL-2-PHENYLTHIAZOLE
    • 1826-17-1
    • DTXSID70338903
    • Thiazole, 4-methyl-2-phenyl-
    • AKOS015899564
    • SCHEMBL87128
    • CS-0129073
    • CS-10955
    • Q63408916
    • IPOHWQDCODUHTD-UHFFFAOYSA-N
    • DA-39135
    • G87014
    • MDL: MFCD00272328
    • Inchi: 1S/C10H9NS/c1-8-7-12-10(11-8)9-5-3-2-4-6-9/h2-7H,1H3
    • InChI Key: IPOHWQDCODUHTD-UHFFFAOYSA-N
    • SMILES: S1C=C(C)N=C1C1C=CC=CC=1

Computed Properties

  • Exact Mass: 175.04600
  • Monoisotopic Mass: 175.04557
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 143
  • 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: nothing
  • XLogP3: 3
  • Topological Polar Surface Area: 41.1

Experimental Properties

  • Color/Form: liquid
  • Density: 1.14
  • Boiling Point: 296.5°C at 760 mmHg
  • Flash Point: 136.9°C
  • Refractive Index: 1.6270
  • PSA: 41.13000
  • LogP: 3.11850
  • Solubility: Insoluble in water

4-Methyl-2-phenylthiazole Security Information

4-Methyl-2-phenylthiazole 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%

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4-Methyl-2-phenylthiazole Related Literature

Additional information on 4-Methyl-2-phenylthiazole

Recent Advances in the Study of 4-Methyl-2-phenylthiazole (CAS: 1826-17-1) in Chemical Biology and Pharmaceutical Research

4-Methyl-2-phenylthiazole (CAS: 1826-17-1) is a heterocyclic compound that has garnered significant attention in recent years due to its potential applications in chemical biology and pharmaceutical research. This compound, characterized by a thiazole ring substituted with a phenyl group and a methyl group, has been the subject of numerous studies aimed at exploring its biological activities, synthetic pathways, and therapeutic potential. The latest research highlights its role as a versatile scaffold in drug discovery, particularly in the development of anti-inflammatory, antimicrobial, and anticancer agents.

Recent studies have focused on the synthesis and optimization of 4-Methyl-2-phenylthiazole derivatives to enhance their pharmacological properties. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated that certain derivatives of this compound exhibit potent inhibitory effects on cyclooxygenase-2 (COX-2), a key enzyme involved in inflammatory processes. The researchers employed molecular docking and in vitro assays to identify the most promising candidates, paving the way for further preclinical evaluations.

In addition to its anti-inflammatory potential, 4-Methyl-2-phenylthiazole has shown promise as an antimicrobial agent. A 2022 study in Bioorganic & Medicinal Chemistry Letters reported that derivatives of this compound exhibited significant activity against a range of Gram-positive and Gram-negative bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). The study attributed this activity to the compound's ability to disrupt bacterial cell membrane integrity, suggesting a novel mechanism of action that could be exploited to combat antibiotic-resistant pathogens.

The anticancer potential of 4-Methyl-2-phenylthiazole has also been a focal point of recent research. A 2023 paper in European Journal of Medicinal Chemistry explored the compound's ability to induce apoptosis in cancer cells by targeting specific signaling pathways, such as the PI3K/Akt/mTOR axis. The study highlighted the compound's selectivity for cancer cells over normal cells, a critical factor in reducing off-target effects and improving therapeutic outcomes. These findings underscore the potential of 4-Methyl-2-phenylthiazole as a lead compound for the development of targeted cancer therapies.

Beyond its pharmacological applications, 4-Methyl-2-phenylthiazole has also been investigated for its role in chemical biology. A 2023 study in ACS Chemical Biology utilized this compound as a fluorescent probe to study protein-ligand interactions in real time. The researchers demonstrated that the compound's unique photophysical properties make it an excellent tool for visualizing dynamic biological processes, offering new insights into cellular mechanisms and drug-target interactions.

In conclusion, the latest research on 4-Methyl-2-phenylthiazole (CAS: 1826-17-1) highlights its multifaceted potential in chemical biology and pharmaceutical research. From its anti-inflammatory and antimicrobial properties to its applications in cancer therapy and chemical probes, this compound continues to be a valuable asset in the quest for novel therapeutics and biological tools. Future studies are expected to further elucidate its mechanisms of action and optimize its derivatives for clinical applications, solidifying its place in the forefront of modern drug discovery.

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