structure of 3,8-Bis(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-1,10-phenanthroline

3,8-Bis(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-1,10-phenanthroline

CAS No.: 1001330-07-9
M. Wt: 460.52500
M. Fa: C24H16N2O4S2
InChI Key: NNNJFZNRZQYNOQ-UHFFFAOYSA-N

Names and Identifiers of 1001330-07-9

CAS Number

1001330-07-9

MDL Number

MFCD27923030

IUPAC Name

3,8-bis({2H,3H-thieno[3,4-b][1,4]dioxin-5-yl})-1,10-phenanthroline

InChI

InChI=1S/C24H16N2O4S2/c1-2-14-8-16(24-22-18(12-32-24)28-4-6-30-22)10-26-20(14)19-13(1)7-15(9-25-19)23-21-17(11-31-23)27-3-5-29-21/h1-2,7-12H,3-6H2

InChIKey

NNNJFZNRZQYNOQ-UHFFFAOYSA-N

Canonical SMILES

C1=CC2=C(N=CC(C3=C4OCCOC4=CS3)=C2)C2=NC=C(C3=C4OCCOC4=CS3)C=C12

UNSPSC Code

12352100

Physical and chemical properties of 1001330-07-9

Exact Mass

460.05500

H Bond Acceptors

6

H Bond Donors

0

LogP

5.78240

Molecular Formula

C24H16N2O4S2

Molecular Weight

460.52500

PSA

119.18000

Safety Information of 1001330-07-9

Pictograms

Signal Word

 Warning

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of 1001330-07-9

The unique properties of 3,8-Bis(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-1,10-phenanthroline make it applicable in several fields:

  • Organic Electronics: Its ability to conduct electricity makes it suitable for use in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs).
  • Sensors: The compound can be utilized in the development of chemical sensors due to its interaction with metal ions.
  • Photovoltaics: Its optical properties can be harnessed in solar energy conversion technologies.

Interaction Studies of 1001330-07-9

Interaction studies involving 3,8-Bis(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-1,10-phenanthroline focus on its binding affinity with various metal ions and biological macromolecules:

  • Metal Ion Coordination: Research indicates that the compound can form stable complexes with transition metals like copper and nickel.
  • DNA Interaction: Studies suggest that it can intercalate into DNA structures, which is significant for drug design and molecular biology applications.

These interactions not only elucidate the compound's potential biological effects but also provide insights into its utility in coordination chemistry.

Biological Activity of 1001330-07-9

Preliminary studies suggest that 3,8-Bis(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-1,10-phenanthroline may exhibit biological activity due to its structural features. Compounds with similar structures have shown:

  • Antimicrobial Properties: Some derivatives have demonstrated effectiveness against various bacterial strains.
  • Anticancer Activity: Certain phenanthroline derivatives have been studied for their potential to inhibit cancer cell proliferation.
  • DNA Binding: The ability to intercalate into DNA suggests potential applications in gene therapy and molecular diagnostics.