6641-96-9

Usage

Molecular structure

A complex structure consisting of a thiazole ring fused with another thiazole ring and two phenyl groups attached to the 2 and 5 positions of the thiazole rings.

Type of compound

A chemical compound belonging to the class of thiazoles.

Unique value

Its unique structure makes it a valuable target for chemical synthesis and research into its properties and potential uses.

Position of phenyl groups

The two phenyl groups are attached to the 2 and 5 positions of the thiazole rings, which may influence its electronic and optical properties.

Fusion of rings

The fusion of the two thiazole rings in the structure contributes to the compound's stability and potential applications in electronic materials.

Electronic and optical properties

The specific electronic and optical properties of 2,5-diphenyl[1,3]thiazolo[5,4-d][1,3]thiazole have not been provided, but they are likely to be unique and of interest for research and potential applications.

Upstream product

• 100-52-7 benzaldehyde 
• 79-40-3 dithiooxamide 

Downstream Products

• 4402-40-8 2,5-bis(4-nitrophenyl)[1,3]thiazolo[5,4-d][1,3]thiazole 
• 4416-79-9 4,4'-(thiazolo[5,4-d]thiazole-2,5-diyl)dianiline 

Relevant academic research and scientific papers

Synthesis and spectroscopic-voltammetric behaviors of silver(I) 2,5-diphenylthiazolo[5,4-d]thiazole

In the present work, 2,5-diphenylthiazolo[5,4-d]thiazole (DTT) and silver(I) 2,5-diphenylthiazolo[5,4-d]thiazole complex(Ag2DTT) were synthesized, and then their spectroscopic and voltammetric behaviors were investigated. The DTT was obtained b

Synthesis, optical dye properties and band gap energies of silver hydroxy-aryl thiazolo[5,4-d]thiazole complexes

In the present work, phenyl-, o?hydroxy phenyl-, o,p?hydroxy phenyl-, p?hydroxy phenyl- and o?hydroxy naphtyl-thiazolo[5,4-d]thiazole dye molecules and their silver complexes were synthesized. The optical microscopy, UV–vis. absorption spectroscopy, FT-IR

Exploration of Thiazolo[5,4-d]thiazole Linkages in Conjugated Porous Organic Polymers for Chemoselective Molecular Sieving

Porous organic polymers (POPs) have attracted significant attention towards molecular adsorption in recent years due to their high porosity, diverse functionality and excellent chemical stability. In this work, we present a systematic case study on the fo

Microwave-assisted synthesis of 2,5-diarylthiazolo[5,4-d]thiazoles from benzaldehydes and dithiooxamide

One-pot condensation of dithiooxamide with aromatic aldehydes and subsequent oxidation of intermediate 2,5-dihydro[1,3]thiazolo[5,4-d][1,3]thiazoles with selenium dioxide afforded 2,6-diaryl[1,3]thiazolo-[5,4-d][1,3]thiazoles which were characterized by

Microwave-activated synthesis of thiazolo[5,4-d]thiazoles by a condensation/oxidation sequence

A microwave-assisted preparation of symmetrical thiazolo[5,4-d]thiazoles from the corresponding aldehydes is presented. The two-step reaction sequence comprises the condensation of aldehydes with dithiooxamide followed by oxidation/aromatization with 1,4-

Diboron-containing fluorophores with extended ladder-type π-conjugated skeletons

A series of ladder type π-conjugated diboron complexes 1-4 have been designed and synthesized by a very simple synthetic procedure. Single crystals of complex 3 were grown and the molecular structure determined by X-ray diffraction analysis demonstrated t