Cas no 72121-34-7 (4-Pyridinecarboxylic acid, 1,2-ethanediyl ester)

4-Pyridinecarboxylic acid, 1,2-ethanediyl ester is a specialized organic compound featuring a pyridine core linked to a carboxylic acid ester group via an ethylene bridge. This structure imparts unique reactivity, making it valuable as an intermediate in pharmaceutical and agrochemical synthesis. Its ester functionality enhances solubility in organic solvents, facilitating reactions such as nucleophilic substitutions or cross-couplings. The pyridine moiety contributes to coordination properties, potentially useful in catalyst design or metal-organic frameworks. The ethylene spacer offers flexibility, enabling tailored modifications for target applications. Careful handling is advised due to potential sensitivity to hydrolysis under acidic or basic conditions.
4-Pyridinecarboxylic acid, 1,2-ethanediyl ester structure
72121-34-7 structure
Product Name:4-Pyridinecarboxylic acid, 1,2-ethanediyl ester
CAS No:72121-34-7
MF:C14H12N2O4
MW:272.256083488464
CID:544478
Update Time:2025-05-24

4-Pyridinecarboxylic acid, 1,2-ethanediyl ester Chemical and Physical Properties

Names and Identifiers

    • 4-Pyridinecarboxylic acid, 1,2-ethanediyl ester
    • Inchi: 1S/C14H12N2O4/c17-13(11-1-5-15-6-2-11)19-9-10-20-14(18)12-3-7-16-8-4-12/h1-8H,9-10H2
    • InChI Key: NGBHSNYNHWOVBX-UHFFFAOYSA-N
    • SMILES: O(C(C1C=CN=CC=1)=O)CCOC(C1C=CN=CC=1)=O

Computed Properties

  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 7

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Additional information on 4-Pyridinecarboxylic acid, 1,2-ethanediyl ester

Recent Advances in the Study of 4-Pyridinecarboxylic acid, 1,2-ethanediyl ester (CAS: 72121-34-7)

4-Pyridinecarboxylic acid, 1,2-ethanediyl ester (CAS: 72121-34-7) is a chemical compound of significant interest in the field of chemical biology and pharmaceutical research. This compound, characterized by its pyridine core and ester linkage, has been the subject of recent investigations due to its potential applications in drug development and biochemical studies. The unique structural features of this molecule make it a promising candidate for various therapeutic and diagnostic applications.

Recent studies have focused on the synthesis and characterization of 4-Pyridinecarboxylic acid, 1,2-ethanediyl ester, with particular emphasis on its reactivity and stability under different conditions. Researchers have employed advanced spectroscopic techniques, including NMR and mass spectrometry, to elucidate its molecular structure and confirm its purity. These efforts are crucial for ensuring the reproducibility of experiments and the reliability of subsequent biological assays.

One of the key findings in recent literature is the role of 4-Pyridinecarboxylic acid, 1,2-ethanediyl ester as a building block in the synthesis of more complex pharmaceutical agents. Its ability to act as a linker or spacer in drug conjugates has been explored, with promising results in enhancing drug delivery and targeting efficiency. Additionally, its potential as a modulator of enzymatic activity has been investigated, opening new avenues for the development of enzyme inhibitors.

In the context of biomedical applications, 4-Pyridinecarboxylic acid, 1,2-ethanediyl ester has shown promise in the design of prodrugs. Prodrug strategies leverage the compound's ester functionality to improve the pharmacokinetic properties of active pharmaceutical ingredients. Recent studies have demonstrated its utility in enhancing the bioavailability and reducing the toxicity of certain therapeutic agents, making it a valuable tool in modern drug design.

Another area of interest is the compound's potential use in diagnostic imaging. Researchers have explored its incorporation into contrast agents for medical imaging techniques such as MRI and PET. The pyridine moiety's ability to coordinate with metal ions has been exploited to develop novel imaging probes with improved sensitivity and specificity. These advancements hold significant promise for early disease detection and monitoring.

Despite these promising developments, challenges remain in the large-scale production and application of 4-Pyridinecarboxylic acid, 1,2-ethanediyl ester. Issues such as scalability of synthesis, cost-effectiveness, and regulatory compliance need to be addressed to facilitate its transition from the laboratory to clinical use. Ongoing research aims to optimize synthetic routes and evaluate the compound's safety profile in preclinical models.

In conclusion, 4-Pyridinecarboxylic acid, 1,2-ethanediyl ester (CAS: 72121-34-7) represents a versatile and valuable compound in chemical biology and pharmaceutical research. Its unique structural properties and diverse applications make it a focal point of current investigations. Continued research efforts are expected to further elucidate its potential and overcome existing challenges, paving the way for its broader utilization in medicine and biotechnology.

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