1033-90-5

Usage

General Description

2,5-DIPHENYL-1,6,6A-TRITHIAPENTALENE is a chemical compound with the molecular formula C20H16S3. It is a trithiapentalene derivative with three sulfur atoms and a five-membered ring. The compound is primarily used in research and development as a building block for organic synthesis and materials science. It has potential applications in the development of new organic electronic materials, such as organic light-emitting diodes and organic photovoltaics, due to its unique structural and electronic properties. Additionally, its aromatic nature and sulfur-containing functional groups make it of interest for chemical and pharmaceutical research. However, it is important to handle and use 2,5-DIPHENYL-1,6,6A-TRITHIAPENTALENE with caution due to its potential health hazards and safety concerns.

InChI:InChI=1/C17H12S3/c1-3-7-13(8-4-1)16-11-15-12-17(19-20(15)18-16)14-9-5-2-6-10-14/h1-12H

Upstream product

• 53344-27-7 2-Phenylcyclopropenone 
• 107451-76-3 1,5-diphenylpent-1-yne-3,5-dione 
• 29179-25-7 cinnamylideneacetophenone 

Downstream Products

• 25576-82-3 4-benzhydrylidene-2,6-diphenyl-4H-thiopyran 
• 632-51-9 1,1,2,2-tetraphenylethylene 
• 87057-27-0 6-Phenyl-4-[2-phenyl-2-thioxo-eth-(Z)-ylidene]-4H-[1,3,2]dithiazine-2-carboxylic acid ethyl ester 
• 87057-34-9 (E)-3-(9-Hydroxy-2-phenyl-naphtho[2,3-b]thiophen-4-yl)-1,3-diphenyl-propenone 

Related news

Photophysical properties of 2,5-DIPHENYL-1,6,6A-TRITHIAPENTALENE (cas 1033-90-5) revealed by time-resolved spectroscopy07/22/2019

The fluorescence decay from S2(π, π*) state of 2,5-diphenyl-1,6,6a-trithiapentalene (DP-TTP) in cyclohexane, tetrahydrofuran and acetonitrile solutions of a quantum yield of ∼0.02–0.04 were measured. The results indicate that, the dominant process of radiationless deactivation of the S2 stat...detailed

Relevant academic research and scientific papers

Selective [3 + 2] Cycloaddition of Cyclopropenone Derivatives and Elemental Chalcogens

A highly efficient method is disclosed for the synthesis of 1,2-dichalcogen heterocycles via [3 + 2] cycloaddition of cyclopropenone derivatives and elemental chalcogens. Different from other cyclopropenone derivatives, cyclopropenselenones undergo unprec

The reaction of unsaturated carbonyl compounds with "activated" sulfur

In a reinvestigation of the sulfuration reaction of cinnamylideneacetophenone (1) with sulfur and triethylamine at room temperature, new products 6-benzoyl-3-phenyl-1,2-dithiolo1,2-dithiole (5), 6-benzoyl-3-phenyl-1,2-dithiine (6) and 5-benzoyl-3-b

A NEW SYNTHESIS OF 6-THIATHIOPHTHENES FROM ACETYLENIC β-DIKETONES

A new method for the synthsis of 2,5-diaryl-6-thiathiophthenes is described involving the reaction of 1,5-diarylpent-1-yne-3,5-diones with phosphorus pentasulfide.The reaction of 3-chloro-6-thiathiophthenes with hydrazine hydrate gave pyrazole derivatives