Cas no 19774-97-1 (2-(4-Chloro-2-cyclohexylphenoxy)acetic acid)

2-(4-Chloro-2-cyclohexylphenoxy)acetic acid is a substituted phenoxyacetic acid derivative with potential applications in organic synthesis and agrochemical research. Its structure features a cyclohexyl group and a chloro substituent on the aromatic ring, contributing to its unique steric and electronic properties. This compound may serve as a key intermediate in the development of herbicides or plant growth regulators due to its structural similarity to biologically active phenoxy acids. The presence of both hydrophobic (cyclohexyl) and polar (carboxylic acid) functional groups enhances its versatility in chemical modifications. Its well-defined molecular architecture allows for precise reactivity in targeted synthetic pathways, making it a valuable building block in specialized organic transformations.
2-(4-Chloro-2-cyclohexylphenoxy)acetic acid structure
19774-97-1 structure
Product Name:2-(4-Chloro-2-cyclohexylphenoxy)acetic acid
CAS No:19774-97-1
MF:C14H17ClO3
MW:268.735983610153
CID:908407
Update Time:2025-11-02

2-(4-Chloro-2-cyclohexylphenoxy)acetic acid Chemical and Physical Properties

Names and Identifiers

    • (4-chloro-2-cyclohexylphenoxy)acetic acid
    • acetic acid, 2-(4-chloro-2-cyclohexylphenoxy)-
    • 2-(4-chloro-2-cyclohexylphenoxy)acetic acid
    • 2-(4-Chloro-2-cyclohexylphenoxy)acetic acid
    • Inchi: 1S/C14H17ClO3/c15-11-6-7-13(18-9-14(16)17)12(8-11)10-4-2-1-3-5-10/h6-8,10H,1-5,9H2,(H,16,17)
    • InChI Key: OGVODSDQXYUSDP-UHFFFAOYSA-N
    • SMILES: ClC1C=CC(=C(C=1)C1CCCCC1)OCC(=O)O

Computed Properties

  • Exact Mass: 268.08671

Experimental Properties

  • PSA: 46.53

2-(4-Chloro-2-cyclohexylphenoxy)acetic acid Pricemore >>

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Additional information on 2-(4-Chloro-2-cyclohexylphenoxy)acetic acid

Recent Advances in the Study of 2-(4-Chloro-2-cyclohexylphenoxy)acetic Acid (CAS: 19774-97-1)

The compound 2-(4-Chloro-2-cyclohexylphenoxy)acetic acid (CAS: 19774-97-1) has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This molecule, characterized by its unique structural features, has shown promising potential in various therapeutic applications. Recent studies have focused on elucidating its mechanism of action, optimizing its synthesis, and exploring its pharmacological properties. This research brief aims to provide an overview of the latest findings related to this compound, highlighting its significance in drug development and chemical biology.

One of the key areas of investigation has been the synthesis and structural modification of 2-(4-Chloro-2-cyclohexylphenoxy)acetic acid. Researchers have developed novel synthetic routes to improve yield and purity, which are critical for its application in drug discovery. Advanced techniques such as high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy have been employed to characterize the compound and its derivatives. These efforts have led to the identification of more efficient and scalable synthesis methods, facilitating further research and potential commercialization.

In addition to synthetic advancements, recent studies have explored the biological activity of 2-(4-Chloro-2-cyclohexylphenoxy)acetic acid. Preliminary findings suggest that this compound exhibits notable anti-inflammatory and analgesic properties, making it a candidate for the development of new therapeutics for chronic pain and inflammatory diseases. Mechanistic studies have indicated that the compound may modulate key signaling pathways involved in inflammation, such as the NF-κB pathway. These insights provide a foundation for future research aimed at optimizing its pharmacological profile and minimizing potential side effects.

Another promising avenue of research involves the potential application of 2-(4-Chloro-2-cyclohexylphenoxy)acetic acid in oncology. Recent in vitro and in vivo studies have demonstrated its ability to inhibit the proliferation of certain cancer cell lines, particularly those associated with solid tumors. The compound's ability to induce apoptosis and suppress angiogenesis has been a focal point of these investigations. While these findings are preliminary, they underscore the compound's potential as a lead molecule for anticancer drug development.

Despite these encouraging results, challenges remain in the development of 2-(4-Chloro-2-cyclohexylphenoxy)acetic acid as a therapeutic agent. Issues such as bioavailability, metabolic stability, and toxicity profiles need to be addressed through further preclinical and clinical studies. Collaborative efforts between academic institutions and pharmaceutical companies will be essential to overcome these hurdles and translate the compound's potential into viable treatments.

In conclusion, 2-(4-Chloro-2-cyclohexylphenoxy)acetic acid (CAS: 19774-97-1) represents a promising candidate for drug development, with applications spanning anti-inflammatory, analgesic, and anticancer therapies. Continued research into its synthesis, mechanism of action, and pharmacological properties will be crucial for unlocking its full therapeutic potential. This research brief highlights the importance of interdisciplinary collaboration and innovative approaches in advancing the field of chemical biology and pharmaceutical sciences.

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