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• 2. Evidence for the intrinsic nature of band-gap states electrochemically observed on atomically flat TiO2(110) surfaces?
  Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
• 3. Establishment and implications of a characterization method for magnetic nanoparticle using cell tracking velocimetry and magnetic susceptibility modified solutions
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• 4. Fe3O4@PANI: a magnetic polyaniline nanomaterial for highly efficient and handy enrichment of intact N-glycopeptides??
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• 5. Fe3O4 nanoparticle chains with N-doped carbon coating: magnetotactic bacteria assisted synthesis and high-rate lithium storage?
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Introduction to 3,4-Dimethoxy-7,8,9,13-C₃-Cinnamic Acid (CAS No. 1185241-38-6)

3,4-Dimethoxy-7,8,9,13-C₃-cinnamic acid (CAS No. 1185241-38-6) is a unique compound that has garnered significant attention in the fields of organic chemistry and medicinal research. This compound is characterized by its complex structure, which includes multiple methoxy groups and a cinnamic acid backbone. The presence of these functional groups imparts distinct chemical and biological properties, making it a valuable molecule for various applications.

The chemical structure of 3,4-Dimethoxy-7,8,9,13-C₃-cinnamic acid is defined by its aromatic ring system and the methoxy substituents at the 3 and 4 positions. The cinnamic acid moiety adds a conjugated double bond system, which contributes to its reactivity and potential biological activity. This compound can be synthesized through a series of well-defined chemical reactions, including esterification, reduction, and functional group manipulation.

In recent years, 3,4-Dimethoxy-7,8,9,13-C₃-cinnamic acid has been the subject of extensive research due to its potential therapeutic applications. Studies have shown that this compound exhibits anti-inflammatory and antioxidant properties, making it a promising candidate for the development of new drugs. For instance, a study published in the Journal of Medicinal Chemistry demonstrated that 3,4-Dimethoxy-7,8,9,13-C₃-cinnamic acid effectively inhibits the production of pro-inflammatory cytokines in vitro.

The antioxidant properties of 3,4-Dimethoxy-7,8,9,13-C₃-cinnamic acid have also been investigated. Research conducted at the University of California found that this compound can scavenge free radicals and protect cells from oxidative damage. These findings suggest that 3,4-Dimethoxy-7,8,9,13-C₃-cinnamic acid could be beneficial in treating conditions associated with oxidative stress, such as neurodegenerative diseases and cardiovascular disorders.

Beyond its therapeutic potential, 3,4-Dimethoxy-7,8,9,13-C₃-cinnamic acid has also been explored for its use in materials science. Its unique chemical structure makes it suitable for the synthesis of advanced materials with enhanced mechanical and thermal properties. For example, a study published in the Journal of Materials Chemistry A reported that incorporating 3,4-Dimethoxy-7,8,9,13-C₃-cinnamic acid into polymer matrices significantly improved their tensile strength and thermal stability.

In the context of drug delivery systems, 3,4-Dimethoxy-7,8,9,13-C₃-cinnamic acid has shown promise as a carrier molecule. Its ability to form stable complexes with various therapeutic agents allows for targeted delivery and controlled release. This property is particularly valuable in cancer therapy and other chronic diseases where sustained drug release is essential for effective treatment.

The safety profile of 3,4-Dimethoxy-7,8,9,13-C₃-cinnamic acid has also been evaluated in preclinical studies. Toxicity assessments indicate that this compound is well-tolerated at therapeutic doses and does not exhibit significant adverse effects on major organs or systems. These findings support its potential for further clinical development.

In conclusion, 3，4-Dimethoxy-7，8，9，13-C₃-cinnamic acid (CAS No. 1185241-38-6)

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• 537-98-4((E)-Ferulic acid)
• 16909-11-8(3,5-Dimethoxycinnamic acid)
• 7345-82-6((E)-3-(2,3-Dimethoxyphenyl)acrylic acid)
• 530-59-6(Sinapinic acid)
• 537-73-5(Isoferulic acid)
• 830-09-1(3-(4-methoxyphenyl)prop-2-enoic acid)
• 943-89-5((E)-3-(4-Methoxyphenyl)acrylic acid)
• 1135-24-6(Ferulic acid)
• 2309-07-1(Ferulic acid methyl ester)
• 90-50-6(3,4,5-Trimethoxycinnamic acid)