Cas no 1730-43-4 (3,7-dimethoxy-10H-phenothiazine)

3,7-Dimethoxy-10H-phenothiazine is a substituted phenothiazine derivative characterized by methoxy functional groups at the 3- and 7-positions. This heterocyclic compound exhibits notable electronic and photophysical properties, making it a valuable intermediate in organic synthesis and materials science. Its rigid, planar structure and electron-rich nature contribute to its utility in the development of optoelectronic materials, including organic semiconductors and fluorescent dyes. The methoxy substituents enhance solubility in common organic solvents, facilitating further chemical modifications. Additionally, its redox-active core lends potential applications in charge-transport materials or as a building block for pharmacologically active compounds. The compound's stability and well-defined reactivity profile support its use in controlled synthetic transformations.
3,7-dimethoxy-10H-phenothiazine structure
1730-43-4 structure
Product Name:3,7-dimethoxy-10H-phenothiazine
CAS No:1730-43-4
MF:C14H13NO2S
MW:259.32352232933
MDL:MFCD00445411
CID:1361489
PubChem ID:621196
Update Time:2025-05-24

3,7-dimethoxy-10H-phenothiazine Chemical and Physical Properties

Names and Identifiers

    • 10H-Phenothiazine, 3,7-dimethoxy-
    • 3,7-dimethoxy-10H-phenothiazine
    • 1730-43-4
    • 3,7-dimethoxy-phenothiazine
    • DTXSID70347414
    • EN300-23811747
    • Z56754477
    • CHEMBL2063785
    • BDBM50389292
    • Oprea1_773697
    • DB-424306
    • 3,7-Dimethoxyphenothiazine
    • SCHEMBL3489840
    • 3,7-Dimethoxy-10H-phenothiazine #
    • MDL: MFCD00445411
    • Inchi: 1S/C14H13NO2S/c1-16-9-3-5-11-13(7-9)18-14-8-10(17-2)4-6-12(14)15-11/h3-8,15H,1-2H3
    • InChI Key: OZYCUQNWECHWDU-UHFFFAOYSA-N
    • SMILES: S1C2C=C(C=CC=2NC2C=CC(=CC1=2)OC)OC

Computed Properties

  • Exact Mass: 259.06679
  • Monoisotopic Mass: 259.06669983g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 2
  • Complexity: 263
  • 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: 3.6
  • Topological Polar Surface Area: 55.8?2

Experimental Properties

  • PSA: 30.49

3,7-dimethoxy-10H-phenothiazine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Enamine
EN300-23811747-0.05g
3,7-dimethoxy-10H-phenothiazine
1730-43-4 95%
0.05g
$2755.0 2024-06-19

Additional information on 3,7-dimethoxy-10H-phenothiazine

Recent Advances in the Study of 3,7-Dimethoxy-10H-Phenothiazine (CAS: 1730-43-4) and Its Applications in Chemical Biology and Medicine

3,7-Dimethoxy-10H-phenothiazine (CAS: 1730-43-4) is a derivative of phenothiazine, a heterocyclic compound that has garnered significant attention in chemical biology and pharmaceutical research due to its unique structural and electronic properties. Recent studies have explored its potential applications in drug development, photodynamic therapy, and as a building block for advanced materials. This research brief synthesizes the latest findings on this compound, highlighting its mechanisms of action, synthesis methods, and therapeutic potential.

One of the most promising areas of research involves the use of 3,7-dimethoxy-10H-phenothiazine as a photosensitizer in photodynamic therapy (PDT). A 2023 study published in the Journal of Medicinal Chemistry demonstrated that this compound exhibits strong absorption in the visible light spectrum, making it an efficient generator of reactive oxygen species (ROS) upon irradiation. The study further revealed that 3,7-dimethoxy-10H-phenothiazine can selectively target cancer cells, inducing apoptosis with minimal damage to surrounding healthy tissues. These findings suggest its potential as a next-generation PDT agent for treating solid tumors.

In addition to its therapeutic applications, recent research has focused on the synthesis and modification of 3,7-dimethoxy-10H-phenothiazine to enhance its pharmacological properties. A 2024 paper in Organic & Biomolecular Chemistry reported a novel, high-yield synthesis route using palladium-catalyzed C-H activation, which significantly reduces the production of toxic byproducts compared to traditional methods. This advancement is particularly relevant for scaling up production while adhering to green chemistry principles.

The compound's unique electronic structure has also attracted attention in materials science. Researchers at MIT recently incorporated 3,7-dimethoxy-10H-phenothiazine into organic semiconductors, achieving record-high charge carrier mobility in thin-film transistors. This breakthrough, published in Advanced Materials, opens new possibilities for flexible electronics and bioelectronic interfaces.

Despite these advances, challenges remain in the clinical translation of 3,7-dimethoxy-10H-phenothiazine-based therapies. Pharmacokinetic studies indicate that the compound exhibits moderate bioavailability and rapid clearance in vivo. Current research efforts are focused on developing prodrug formulations and nanoparticle delivery systems to overcome these limitations. Preliminary results from animal models show promise, with improved tumor accumulation and reduced systemic toxicity.

In conclusion, 3,7-dimethoxy-10H-phenothiazine (CAS: 1730-43-4) represents a versatile scaffold with applications spanning medicine, materials science, and chemical biology. The compound's photophysical properties, combined with recent synthetic advances, position it as a valuable tool for both therapeutic development and fundamental research. Future studies should prioritize structure-activity relationship investigations and clinical translation efforts to fully realize its potential.

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