Cas no 188493-61-0 (N'1-(3,4,5-trimethoxybenzylidene)-4-methylbenzene-1-sulfonohydrazide)

N'1-(3,4,5-Trimethoxybenzylidene)-4-methylbenzene-1-sulfonohydrazide is a sulfonohydrazide derivative characterized by its trimethoxybenzylidene and methylbenzene sulfonyl functional groups. This compound exhibits potential as an intermediate in organic synthesis, particularly in the development of pharmacologically active molecules due to its structurally versatile scaffold. The presence of electron-donating methoxy groups enhances its reactivity in condensation and cyclization reactions, while the sulfonohydrazide moiety offers opportunities for further functionalization. Its well-defined crystalline structure facilitates purification and characterization, making it suitable for research applications in medicinal chemistry and materials science. The compound's stability under standard conditions ensures reliable handling and storage.
N'1-(3,4,5-trimethoxybenzylidene)-4-methylbenzene-1-sulfonohydrazide structure
188493-61-0 structure
Product Name:N'1-(3,4,5-trimethoxybenzylidene)-4-methylbenzene-1-sulfonohydrazide
CAS No:188493-61-0
MF:C17H20N2O5S
MW:364.416103363037
CID:4626832
Update Time:2025-08-05

N'1-(3,4,5-trimethoxybenzylidene)-4-methylbenzene-1-sulfonohydrazide Chemical and Physical Properties

Names and Identifiers

    • 4-Methyl-N-[(E)-(3,4,5-trimethoxyphenyl)methylideneamino]benzenesulfonamide
    • N'1-(3,4,5-trimethoxybenzylidene)-4-methylbenzene-1-sulfonohydrazide
    • Inchi: 1S/C17H20N2O5S/c1-12-5-7-14(8-6-12)25(20,21)19-18-11-13-9-15(22-2)17(24-4)16(10-13)23-3/h5-11,19H,1-4H3
    • InChI Key: GQELPZMKUNGLPC-UHFFFAOYSA-N
    • SMILES: C1(S(NN=CC2=CC(OC)=C(OC)C(OC)=C2)(=O)=O)=CC=C(C)C=C1

N'1-(3,4,5-trimethoxybenzylidene)-4-methylbenzene-1-sulfonohydrazide Pricemore >>

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Additional information on N'1-(3,4,5-trimethoxybenzylidene)-4-methylbenzene-1-sulfonohydrazide

Research Brief on N'1-(3,4,5-trimethoxybenzylidene)-4-methylbenzene-1-sulfonohydrazide (CAS: 188493-61-0)

N'1-(3,4,5-trimethoxybenzylidene)-4-methylbenzene-1-sulfonohydrazide (CAS: 188493-61-0) is a synthetic sulfonohydrazide derivative that has garnered significant attention in recent years due to its potential applications in medicinal chemistry and drug discovery. This compound, characterized by its unique structural features, has been investigated for its biological activities, particularly in the context of anticancer and anti-inflammatory therapies. The presence of the trimethoxybenzylidene moiety and the sulfonohydrazide group suggests potential interactions with various biological targets, making it a promising candidate for further research.

Recent studies have focused on elucidating the molecular mechanisms underlying the biological effects of this compound. In vitro experiments have demonstrated its ability to inhibit the proliferation of certain cancer cell lines, with preliminary data indicating that it may act through the modulation of key signaling pathways involved in cell cycle regulation and apoptosis. Additionally, its anti-inflammatory properties have been explored, with findings suggesting that it may suppress the production of pro-inflammatory cytokines in immune cells. These results highlight the compound's dual potential as both an anticancer and anti-inflammatory agent.

The synthesis and optimization of N'1-(3,4,5-trimethoxybenzylidene)-4-methylbenzene-1-sulfonohydrazide have also been a focus of recent research. Advances in synthetic methodologies have enabled the production of this compound with higher yields and purity, facilitating more detailed pharmacological evaluations. Structure-activity relationship (SAR) studies have been conducted to identify the critical functional groups responsible for its biological activity, paving the way for the development of more potent analogs.

Despite these promising findings, challenges remain in the development of this compound as a therapeutic agent. Issues such as bioavailability, metabolic stability, and potential off-target effects need to be addressed in future studies. Ongoing research is exploring various formulation strategies, including nanoparticle-based delivery systems, to enhance its pharmacokinetic properties. Furthermore, in vivo studies are needed to validate its efficacy and safety in animal models, which will be crucial for advancing this compound toward clinical trials.

In conclusion, N'1-(3,4,5-trimethoxybenzylidene)-4-methylbenzene-1-sulfonohydrazide represents a promising scaffold for the development of novel therapeutic agents. Its unique chemical structure and demonstrated biological activities make it a valuable subject of investigation in the field of medicinal chemistry. Continued research efforts are expected to further elucidate its mechanisms of action and optimize its pharmacological profile, potentially leading to the discovery of new drugs for the treatment of cancer and inflammatory diseases.

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