Cas no 955976-67-7 (4-ETHYL-3-[(4-METHYLBENZYL)SULFINYL]-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOLE)

4-ETHYL-3-[(4-METHYLBENZYL)SULFINYL]-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOLE is a specialized triazole derivative featuring a sulfinyl and trifluoromethylphenoxy functional group. Its molecular structure imparts unique reactivity, making it valuable in pharmaceutical and agrochemical research, particularly as a potential intermediate or active moiety. The presence of the sulfinyl group enhances polarity and potential binding interactions, while the trifluoromethylphenoxy moiety contributes to metabolic stability and lipophilicity. This compound is suited for applications requiring selective modulation of biological targets, such as enzyme inhibition or receptor binding studies. Its well-defined structure allows for precise modifications, facilitating structure-activity relationship investigations in drug discovery and development.
4-ETHYL-3-[(4-METHYLBENZYL)SULFINYL]-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOLE structure
955976-67-7 structure
Product Name:4-ETHYL-3-[(4-METHYLBENZYL)SULFINYL]-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOLE
CAS No:955976-67-7
MF:C20H20F3N3O2S
MW:423.451913833618
CID:5234531
Update Time:2026-03-08

4-ETHYL-3-[(4-METHYLBENZYL)SULFINYL]-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOLE Chemical and Physical Properties

Names and Identifiers

    • 4-ETHYL-3-[(4-METHYLBENZYL)SULFINYL]-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOLE
    • 4-ETHYL-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOL-3-YL 4-METHYLBENZYL SULFOXIDE
    • 4-ethyl-3-[(4-methylphenyl)methanesulfinyl]-5-{[3-(trifluoromethyl)phenoxy]methyl}-4H-1,2,4-triazole
    • 4H-1,2,4-Triazole, 4-ethyl-3-[[(4-methylphenyl)methyl]sulfinyl]-5-[[3-(trifluoromethyl)phenoxy]methyl]-
    • Inchi: 1S/C20H20F3N3O2S/c1-3-26-18(12-28-17-6-4-5-16(11-17)20(21,22)23)24-25-19(26)29(27)13-15-9-7-14(2)8-10-15/h4-11H,3,12-13H2,1-2H3
    • InChI Key: CTBJQQMEMHHOTG-UHFFFAOYSA-N
    • SMILES: CCN1C(S(CC2C=CC(C)=CC=2)=O)=NN=C1COC1C=C(C(F)(F)F)C=CC=1

4-ETHYL-3-[(4-METHYLBENZYL)SULFINYL]-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOLE Pricemore >>

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4-ETHYL-3-[(4-METHYLBENZYL)SULFINYL]-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOLE Related Literature

Additional information on 4-ETHYL-3-[(4-METHYLBENZYL)SULFINYL]-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOLE

Comprehensive Overview of 4-ETHYL-3-[(4-METHYLBENZYL)SULFINYL]-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOLE (CAS No. 955976-67-7)

The compound 4-ETHYL-3-[(4-METHYLBENZYL)SULFINYL]-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOLE (CAS No. 955976-67-7) is a highly specialized triazole derivative with significant potential in pharmaceutical and agrochemical research. Its unique structural features, including the sulfinyl and trifluoromethylphenoxy moieties, make it a subject of interest for scientists exploring novel bioactive molecules. This article delves into its properties, applications, and relevance in current research trends, addressing common queries from academic and industrial circles.

One of the most frequently searched topics in AI-driven drug discovery is the role of heterocyclic compounds like 1,2,4-triazoles. The 4-ETHYL-3-[(4-METHYLBENZYL)SULFINYL] variant stands out due to its sulfoxide group, which enhances metabolic stability and binding affinity in target interactions. Researchers are particularly intrigued by its potential as a kinase inhibitor or enzyme modulator, aligning with the growing demand for precision medicine solutions.

In the context of agrochemical innovation, this compound’s trifluoromethylphenoxy segment has drawn attention for its pesticidal and herbicidal properties. With global emphasis on sustainable farming, derivatives of 4H-1,2,4-TRIAZOLE are being evaluated for their environmental impact and efficacy against resistant pests. This aligns with searches for "green chemistry alternatives" and "low-toxicity crop protectants."

The synthesis of CAS 955976-67-7 involves multi-step organic reactions, including sulfoxidation and etherification, which are often queried in chemical synthesis forums. Its crystalline form and solubility profile (often in polar aprotic solvents) are critical for formulation studies, a hot topic in pharmaceutical formulation optimization.

From a computational chemistry perspective, the compound’s molecular docking potential is frequently explored. Its electrophilic sites and hydrogen-bonding capacity make it a candidate for virtual screening libraries, addressing the surge in AI-aided drug design inquiries. Researchers also investigate its ADMET (Absorption, Distribution, Metabolism, Excretion, Toxicity) properties, a recurring theme in preclinical development discussions.

In summary, 4-ETHYL-3-[(4-METHYLBENZYL)SULFINYL]-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOLE exemplifies the intersection of medicinal chemistry and material science. Its versatility and relevance to high-impact research areas ensure its continued prominence in scientific literature and patent filings.

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