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4,5-diphenyl-1,2,3-Thiadiazole (CAS 5393-99-7)

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Application:
4,5-diphenyl-1,2,3-Thiadiazole is an antibiotic compound with CYP450 inhibitory properties
CAS Number:
5393-99-7
Molecular Weight:
238.3
Molecular Formula:
C14H10N2S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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4,5-Diphenyl-1,2,3-thiadiazole, listed under CAS number 5393-99-7, is an organic compound that features a thiadiazole ring, a heterocyclic compound containing both sulfur and nitrogen, flanked by two phenyl groups. This chemical structure lends the molecule distinct electronic and optical properties, making it of interest in various research fields, particularly in materials science. The thiadiazole ring is known for its electron-withdrawing nature, which, when combined with the electron-rich phenyl groups, creates a molecule with unique electronic properties conducive to conducting and semiconducting behaviors. This has led to its use in the development and study of organic semiconductor materials, where it contributes to the understanding of charge transport mechanisms in organic electronic devices. The compound′s ability to stabilize charge carriers and facilitate efficient charge transfer makes it a candidate for incorporation into organic light-emitting diodes (OLEDs), photovoltaic cells, and other electronic applications. Research involving 4,5-diphenyl-1,2,3-thiadiazole often focuses on synthesizing and characterizing novel organic electronic materials to explore and optimize their performance in electronic and optoelectronic devices, aiming to enhance device efficiency, stability, and overall performance.


4,5-diphenyl-1,2,3-Thiadiazole (CAS 5393-99-7) References

  1. Photochemical formation of thiirene and thioketene in 1,2,3-thiadiazoles with phenyl substituents studied by time-resolved spectroscopy.  |  Burdzinski, G., et al. 2013. Photochem Photobiol Sci. 12: 895-901. PMID: 23471241
  2. 1,2,3-Thiadiazole: a novel heterocyclic heme ligand for the design of cytochrome P450 inhibitors.  |  Babu, BR. and Vaz, AD. 1997. Biochemistry. 36: 7209-16. PMID: 9188722
  3. DIPHENYLACETYLENE. THE NUCLEOPHILIC RING CLEAVAGE OF 1, 2, 3-THIADIAZOLES.  |  Micetich and R. G. 1971. Organic Preparations and Procedures International. 3.4: 163-166.
  4. Photolysis of 1, 2, 3-thiadiazole. Formation of thiirene by secondary photolysis of thioketene.  |  Larsen and Bjarne Due, et al. 1992. Acta Chem. Scand. 46: 482-486.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4,5-diphenyl-1,2,3-Thiadiazole, 250 mg

sc-205127
250 mg
$20.00

4,5-diphenyl-1,2,3-Thiadiazole, 500 mg

sc-205127A
500 mg
$34.00