Cas no 259139-19-0 (3,4-(2',2'-diethylpropylene)dioxythiophene)

3,4-(2',2'-Diethylpropylene)dioxythiophene is a specialized derivative of 3,4-ethylenedioxythiophene (EDOT), featuring diethylpropylene bridging groups. This modification enhances the compound's electronic and structural properties, making it particularly valuable in the development of conductive polymers and organic electronic materials. Its extended conjugated system improves charge carrier mobility, while the diethylpropylene substituents contribute to solubility and processability in organic solvents. These characteristics make it a promising monomer for synthesizing high-performance conducting polymers used in applications such as organic thin-film transistors, electrochromic devices, and flexible electronics. The compound’s stability and tunable electronic properties further underscore its utility in advanced material research.
3,4-(2',2'-diethylpropylene)dioxythiophene structure
259139-19-0 structure
Product Name:3,4-(2',2'-diethylpropylene)dioxythiophene
CAS No:259139-19-0
MF:C11H16O2S
MW:212.308542251587
MDL:MFCD08705267
CID:914124
PubChem ID:24885029
Update Time:2025-10-23

3,4-(2',2'-diethylpropylene)dioxythiophene Chemical and Physical Properties

Names and Identifiers

    • 3,4-(2',2'-diethylpropylene)dioxythiophene
    • 3,3-diethyl-2,4-dihydrothieno[3,4-b][1,4]dioxepine
    • 3,4-(2′,2′-Diethylpropylene)dioxythiophene
    • 2H-Thieno[3,4-b][1,4]dioxepin, 3,3-diethyl-3,4-dihydro-
    • 3,3-Diethyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepin
    • 3,3-diethyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine
    • 3,4-(2 inverted exclamation marka,2 inverted exclamation marka-Diethylpropylene)dioxythiophene
    • 3,4-(2,2-diethylpropane-1,3-diyldioxy)thiophene
    • 669210_ALDRICH
    • AG-E-80360
    • AGN-PC-00F3Z8
    • CTK0J3698
    • SureCN2754120
    • J-016176
    • 3,4-(2,2-Diethylpropylene)dioxythiophene,97%
    • SB67116
    • SCHEMBL2754120
    • CS-0450451
    • 3,3-DIETHYL-2H,4H-THIENO[3,4-B][1,4]DIOXEPINE
    • DTXSID90471346
    • 259139-19-0
    • 3,4-(2',2'-Diethylpropylene)dioxythiophene, 97%
    • MFCD08705267
    • MDL: MFCD08705267
    • Inchi: 1S/C11H16O2S/c1-3-11(4-2)7-12-9-5-14-6-10(9)13-8-11/h5-6H,3-4,7-8H2,1-2H3
    • InChI Key: HMKHKPKUPVRLOW-UHFFFAOYSA-N
    • SMILES: S1C=C2C(=C1)OCC(CO2)(CC)CC

Computed Properties

  • Exact Mass: 212.08700
  • Monoisotopic Mass: 212.08710092g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 176
  • 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: 3.2
  • Topological Polar Surface Area: 46.7?2

Experimental Properties

  • Density: 1.109?g/mL?at 25?°C
  • Refractive Index: n20/D 1.534
  • PSA: 46.70000
  • LogP: 3.32570

3,4-(2',2'-diethylpropylene)dioxythiophene Security Information

  • Hazardous Material transportation number:NONH for all modes of transport
  • WGK Germany:3

3,4-(2',2'-diethylpropylene)dioxythiophene Pricemore >>

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Additional information on 3,4-(2',2'-diethylpropylene)dioxythiophene

Recent Advances in the Study of 259139-19-0 and 3,4-(2',2'-Diethylpropylene)dioxythiophene in Chemical Biomedicine

The compound 259139-19-0 and its derivative, 3,4-(2',2'-diethylpropylene)dioxythiophene, have recently garnered significant attention in the field of chemical biomedicine due to their unique structural properties and potential therapeutic applications. This research brief aims to synthesize the latest findings on these compounds, focusing on their synthesis, biological activity, and potential applications in drug development and biomedical engineering.

Recent studies have highlighted the role of 259139-19-0 as a key intermediate in the synthesis of novel conjugated polymers, particularly those based on thiophene derivatives. The compound's structural versatility allows for the development of materials with tailored electronic and optical properties, making it a promising candidate for applications in biosensors and drug delivery systems. Concurrently, 3,4-(2',2'-diethylpropylene)dioxythiophene has been investigated for its exceptional conductivity and biocompatibility, which are critical for its use in neural interfaces and tissue engineering scaffolds.

One of the most notable advancements in this area is the successful integration of 3,4-(2',2'-diethylpropylene)dioxythiophene into organic electrochemical transistors (OECTs). These devices have demonstrated remarkable sensitivity in detecting biomolecules, such as glucose and dopamine, at physiologically relevant concentrations. The high stability and low cytotoxicity of this polymer under physiological conditions further underscore its potential for in vivo applications. Additionally, researchers have explored its use in photodynamic therapy, where its ability to generate reactive oxygen species upon light irradiation has shown promise in targeted cancer treatment.

From a synthetic chemistry perspective, novel methodologies have been developed to optimize the production of 259139-19-0 and its derivatives. Recent publications describe improved catalytic systems that enhance yield and purity while reducing environmental impact. These advances are particularly relevant given the growing demand for sustainable pharmaceutical manufacturing processes. Furthermore, computational studies have provided deeper insights into the structure-activity relationships of these compounds, enabling more rational design of derivatives with enhanced biological activity.

The pharmacological potential of these compounds is equally noteworthy. Preclinical studies have demonstrated that certain derivatives exhibit potent anti-inflammatory and neuroprotective effects, suggesting possible applications in treating neurodegenerative disorders. The unique electronic properties of these molecules also make them suitable candidates for developing novel antimicrobial agents, with preliminary data showing activity against drug-resistant bacterial strains.

In conclusion, the ongoing research on 259139-19-0 and 3,4-(2',2'-diethylpropylene)dioxythiophene continues to reveal exciting possibilities at the intersection of chemistry and biomedicine. While significant progress has been made in understanding their properties and potential applications, further studies are needed to fully explore their therapeutic potential and address challenges related to scalability and long-term biocompatibility. The coming years are likely to witness important developments in this field, potentially leading to breakthrough applications in medical diagnostics and treatment.

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