85344-73-6

Usage

Type of compound

Heterocyclic compound

Structure

Thianthrene derivative with one carbon atom replaced by a nitrogen atom

Physical state

Pale yellow solid

Primary use

Building block in organic synthesis

Potential applications

a. Materials science
b. Organic semiconductors
c. Light-emitting diodes

Biological activity

a. Antimicrobial properties
b. Anticancer properties

Versatility

Potential applications in various fields

Upstream product

• 69212-29-9 3-mercaptopyridin-2(1H)-thione 
• 88-73-3 2-Chloronitrobenzene 
• 2402-77-9 2,3-dichloro-pyridine 
• 17534-15-5 Benzene-1,2-dithiol 

Relevant academic research and scientific papers

Synthesis, Properties, and X-ray Structure of 6-Aza-5,7,12,14-tetrathiapentacene as a Novel Polyheterocyclic Electron Donor, and Related Compounds

Two new compounds, 1-aza-2,3-dichlorothianthrene (5) and 6-aza-5,7,12,14-tetrathiapentacene (6) have been prepared by reaction of 2,3,5,6-tetrachloropyridine (4) and 1,2-benzenedithiol in dimethylformamide (DMF) in the presence of sodium bicarbonate.On th

Chemistry of the Phenoxathiins and Isosterically Related Heterocycles. XXIII. 1-Azathianthrene: First Reported Synthesis of a Monoazathianthrene and the Investigation of the 13C-NMR Spectrum Using Two-dimensional NMR Techniques

The rection of the dianion od 3-mercaptopyridin-2(1H)-thione with 2-chloronitrobenzene in N,N-dimethylformamide leads to the formation of 1-azathianthrene, the first reported mono-aza analog of the thianthrene ring system.A partial assignment of the 13C-nmr spectrum of the title compound is reported, the assignment based on chemical shift arguments, spin-lattice (T1) relaxation times and 1H-13C spin coupling constants.Amplitude modulated two-dimensional Fourier transform (AM2DFT) techniques were employed for the acquisition of the heteronuclear spin-coupling constants.