Cas no 408340-16-9 (Phenol, 2,3-diiodo-)

Phenol, 2,3-diiodo- is a halogenated aromatic compound characterized by the substitution of iodine atoms at the 2 and 3 positions of the phenol ring. This structural modification enhances its reactivity and utility in organic synthesis, particularly in electrophilic substitution and coupling reactions. The presence of iodine imparts increased stability and selectivity, making it valuable for constructing complex molecular frameworks. Its high purity and well-defined reactivity profile ensure consistent performance in pharmaceutical intermediates, agrochemicals, and material science applications. The compound’s distinct electronic properties also facilitate its use in advanced catalytic systems and as a precursor for further functionalization.
Phenol, 2,3-diiodo- structure
Phenol, 2,3-diiodo- structure
Product Name:Phenol, 2,3-diiodo-
CAS No:408340-16-9
MF:C6H4I2O
MW:345.904306411743
MDL:MFCD08166475
CID:326197
PubChem ID:11348539
Update Time:2025-05-25

Phenol, 2,3-diiodo- Chemical and Physical Properties

Names and Identifiers

    • Phenol, 2,3-diiodo-
    • 2,3-DIIODOPHENOL
    • 2,3-DICHLORO-5-BROMOPYRIDINE
    • Phenol,2,3-diiodo
    • Dijodphenol
    • MFCD08166475
    • Q209168
    • SY353146
    • 408340-16-9
    • DTXSID90463180
    • MB05357
    • SCHEMBL605558
    • diiodophenol
    • MDL: MFCD08166475
    • Inchi: 1S/C6H4I2O/c7-4-2-1-3-5(9)6(4)8/h1-3,9H
    • InChI Key: YPJVJVIQWWXEHO-UHFFFAOYSA-N
    • SMILES: IC1C(=CC=CC=1O)I

Computed Properties

  • Exact Mass: 345.83500
  • Monoisotopic Mass: 345.83516g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 0
  • Complexity: 97.1
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.9
  • Topological Polar Surface Area: 20.2?2

Experimental Properties

  • PSA: 20.23000
  • LogP: 2.60140

Phenol, 2,3-diiodo- Pricemore >>

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Additional information on Phenol, 2,3-diiodo-

Recent Advances in the Study of 408340-16-9 and Phenol, 2,3-diiodo-: A Comprehensive Research Brief

In the rapidly evolving field of chemical biology and pharmaceutical research, the compound 408340-16-9 and its derivative, Phenol, 2,3-diiodo-, have garnered significant attention due to their potential applications in drug development and therapeutic interventions. This research brief aims to synthesize the latest findings related to these compounds, providing a detailed overview of their chemical properties, biological activities, and recent advancements in their utilization.

The compound 408340-16-9, a unique chemical entity, has been the subject of numerous studies exploring its role as a precursor or intermediate in the synthesis of bioactive molecules. Recent research has highlighted its utility in the development of novel inhibitors targeting specific enzymatic pathways, particularly those involved in inflammatory and oncogenic processes. The structural versatility of 408340-16-9 allows for modifications that enhance its binding affinity and selectivity, making it a promising candidate for further pharmacological exploration.

Phenol, 2,3-diiodo-, a halogenated phenolic compound, has been investigated for its antimicrobial and antioxidant properties. Studies have demonstrated its efficacy in inhibiting the growth of pathogenic bacteria and fungi, suggesting potential applications in antimicrobial therapies. Additionally, its antioxidant activity has been linked to the scavenging of reactive oxygen species (ROS), which play a critical role in oxidative stress-related diseases. Recent work has focused on optimizing the synthesis of Phenol, 2,3-diiodo- to improve yield and purity, thereby facilitating its broader use in pharmaceutical formulations.

One of the key advancements in this area involves the development of novel synthetic routes for 408340-16-9 and Phenol, 2,3-diiodo-. Researchers have employed advanced catalytic systems and green chemistry principles to enhance the efficiency and sustainability of their production. For instance, the use of palladium-catalyzed cross-coupling reactions has enabled the synthesis of 408340-16-9 with high enantioselectivity, while microwave-assisted techniques have reduced the reaction time for Phenol, 2,3-diiodo- synthesis. These methodological innovations not only improve scalability but also align with the growing emphasis on environmentally friendly chemical processes.

In terms of biological applications, recent in vitro and in vivo studies have shed light on the mechanistic pathways through which 408340-16-9 and Phenol, 2,3-diiodo- exert their effects. For example, 408340-16-9 has been shown to modulate the activity of key signaling proteins, such as kinases and phosphatases, which are implicated in cell proliferation and apoptosis. Phenol, 2,3-diiodo-, on the other hand, has been found to disrupt microbial cell membranes and interfere with redox homeostasis, providing a dual mechanism of action against pathogens. These findings underscore the therapeutic potential of these compounds and warrant further investigation into their clinical applicability.

Despite these promising developments, challenges remain in the translation of these findings into practical applications. Issues such as bioavailability, toxicity, and formulation stability need to be addressed to ensure the safe and effective use of 408340-16-9 and Phenol, 2,3-diiodo- in therapeutic settings. Ongoing research is exploring various drug delivery systems, including nanoparticles and liposomes, to overcome these limitations and enhance the pharmacokinetic profiles of these compounds.

In conclusion, the study of 408340-16-9 and Phenol, 2,3-diiodo- represents a vibrant area of research with significant implications for drug discovery and development. The latest advancements in synthetic methodologies and biological evaluations have expanded our understanding of these compounds and their potential applications. Future research should focus on addressing the remaining challenges and exploring new avenues for their utilization in medicine and biotechnology. This brief serves as a valuable resource for researchers and professionals in the chemical biology and pharmaceutical fields, offering insights into the current state of knowledge and directions for future investigation.

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