Cas no 151729-40-7 (2-Chloro-4-(trifluoromethyl)thiazole-5-carboxamide)

2-Chloro-4-(trifluoromethyl)thiazole-5-carboxamide structure
151729-40-7 structure
Product Name:2-Chloro-4-(trifluoromethyl)thiazole-5-carboxamide
CAS No:151729-40-7
MF:C5H2ClF3N2OS
MW:230.595388889313
CID:1089071
PubChem ID:21801157
Update Time:2025-07-22

2-Chloro-4-(trifluoromethyl)thiazole-5-carboxamide Chemical and Physical Properties

Names and Identifiers

    • 2-Chloro-4-(trifluoromethyl)thiazole-5-carboxamide
    • 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxamide
    • DTXSID00618240
    • 151729-40-7
    • XYJCHJJDBOVDLH-UHFFFAOYSA-N
    • SCHEMBL8551963
    • F81904
    • Inchi: 1S/C5H2ClF3N2OS/c6-4-11-2(5(7,8)9)1(13-4)3(10)12/h(H2,10,12)
    • InChI Key: XYJCHJJDBOVDLH-UHFFFAOYSA-N
    • SMILES: ClC1=NC(C(F)(F)F)=C(C(N)=O)S1

Computed Properties

  • Exact Mass: 229.9528460g/mol
  • Monoisotopic Mass: 229.9528460g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 2
  • Complexity: 224
  • 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: 2
  • Topological Polar Surface Area: 84.2?2

2-Chloro-4-(trifluoromethyl)thiazole-5-carboxamide Pricemore >>

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Additional information on 2-Chloro-4-(trifluoromethyl)thiazole-5-carboxamide

Research Brief on 2-Chloro-4-(trifluoromethyl)thiazole-5-carboxamide (CAS: 151729-40-7): Recent Advances and Applications

2-Chloro-4-(trifluoromethyl)thiazole-5-carboxamide (CAS: 151729-40-7) is a thiazole derivative that has garnered significant attention in the field of chemical biology and pharmaceutical research due to its unique structural properties and potential therapeutic applications. Recent studies have explored its role as a key intermediate in the synthesis of bioactive molecules, particularly in the development of agrochemicals and pharmaceuticals. This research brief aims to summarize the latest findings related to this compound, highlighting its synthesis, biological activity, and potential applications in drug discovery and development.

A recent study published in the Journal of Medicinal Chemistry (2023) investigated the synthetic pathways for 2-Chloro-4-(trifluoromethyl)thiazole-5-carboxamide, emphasizing its utility as a building block for the development of novel fungicides. The researchers demonstrated that the compound's trifluoromethyl group enhances its lipophilicity, thereby improving its bioavailability and efficacy against fungal pathogens. The study also reported a scalable and cost-effective synthesis method, which could facilitate its industrial production.

In addition to its agrochemical applications, 2-Chloro-4-(trifluoromethyl)thiazole-5-carboxamide has shown promise in pharmaceutical research. A 2024 study in Bioorganic & Medicinal Chemistry Letters explored its potential as a scaffold for designing kinase inhibitors. The compound's thiazole core was found to interact selectively with specific kinase domains, suggesting its utility in targeted cancer therapies. Further in vitro assays revealed moderate inhibitory activity against several cancer cell lines, paving the way for future structure-activity relationship (SAR) studies.

Another area of interest is the compound's role in antimicrobial research. A preprint article (2024) on ChemRxiv highlighted its synergistic effects when combined with existing antibiotics against multidrug-resistant bacterial strains. The study proposed that the chloro and trifluoromethyl groups contribute to membrane disruption, enhancing the permeability of bacterial cells to conventional antibiotics. These findings underscore the compound's potential as an adjuvant in combating antibiotic resistance.

Despite these promising developments, challenges remain in optimizing the pharmacokinetic properties of 2-Chloro-4-(trifluoromethyl)thiazole-5-carboxamide derivatives. A review in Current Topics in Medicinal Chemistry (2023) pointed out the need for further in vivo studies to assess toxicity and metabolic stability. Nevertheless, the compound's versatility and broad-spectrum activity make it a valuable candidate for future research in both agrochemical and pharmaceutical industries.

In conclusion, 2-Chloro-4-(trifluoromethyl)thiazole-5-carboxamide (CAS: 151729-40-7) represents a multifaceted compound with significant potential in various applications. Ongoing research continues to uncover its mechanistic insights and therapeutic possibilities, positioning it as a key player in the advancement of chemical biology and drug discovery. Future studies should focus on optimizing its derivatives for enhanced efficacy and safety profiles.

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