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Usage

Uses

Used in Chemical Synthesis Industry:
Phenol,2,2'-thiazolo[5,4-d]thiazole-2,5-diylbis(9CI) is used as a precursor in the synthesis of dyes for its unique chemical structure and reactivity, contributing to the development of novel colorants with specific properties.
Used in Polymer Industry:
In the polymer industry, Phenol,2,2'-thiazolo[5,4-d]thiazole-2,5-diylbis(9CI) is employed as a precursor to create polymers with tailored characteristics, such as enhanced stability or specific functional groups, by incorporating its structure into the polymer backbone.
Used in Pharmaceutical Industry:
Phenol,2,2'-thiazolo[5,4-d]thiazole-2,5-diylbis(9CI) serves as a precursor in the pharmaceutical sector, where its unique chemical properties can be leveraged to develop new drugs with potential therapeutic applications.
Due to the compound's toxicity, it is crucial to implement strict safety measures during its use in these industries to minimize exposure risks and prevent environmental contamination. Continuous research is essential to explore safer alternatives and to better understand the potential applications and associated risks of Phenol,2,2'-thiazolo[5,4-d]thiazole-2,5-diylbis(9CI).

Upstream product

• 90-02-8 salicylaldehyde 
• 79-40-3 dithiooxamide 

Downstream Products

• 1309354-80-0 2,5-bis(2-((diphenylboryl)oxy)phenyl)thiazolo[5,4-d]thiazole 
• 111666-61-6 2-(2-ethoxy-phenyl)-5-(2-methoxy-phenyl)-thiazolo[5,4-d]thiazole 
• 109594-49-2 2-[5-(2-methoxy-phenyl)-thiazolo[5,4-d]thiazol-2-yl]-phenol 
• 111272-34-5 2,5-bis-(2-ethoxy-phenyl)-thiazolo[5,4-d]thiazole 
• 110060-03-2 2-[5-(2-ethoxy-phenyl)-thiazolo[5,4-d]thiazol-2-yl]-phenol 

Relevant academic research and scientific papers

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

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

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-

Boron-bridged π-conjugated ladders as efficient electron-transporting emitters

Four diboron-bridged ladder molecules 1-4 have been designed and synthesized. X-ray diffraction analysis revealed that the bulky phenyl substituents on boron centers efficiently prevented π stacking of the luminescent ladder unit. Characterizations of the

A one-step synthesis towards new ligands based on aryl-functionalised thiazolo[5,4-d]thiazole chromophores

A general synthesis of disubstituted thiazolo[5,4-d]thiazoles was achieved by condensing two equivalents of an aryl aldehyde with dithiooxamide in nitrobenzene at 130 °C for 24 h. The method is tolerant to a range of aromatic aldehydes including derivativ

Thiazolo[5,4-D]thiazsole Color-formers

This invention relates to improved imaging systems based on the formation of green-yellow colored coordination compounds of transition metals with certain ligands. The formation of colored coordination compounds can be employed to generate images and is important in the manufacture and use of pressure sensitive transfer papers for preparing carbonless copies. In particular, this invention relates to certain 2,5-bis(substituted aryl)thiazolo[5,4-d]thiazole compounds, and particularly to certain 2,5-bis(o-hydroxyaryl)thiazolo[5,4-d]thiazole compounds, to their coordination compounds with certain transition metals, and to their use in pressure sensitive carbonless copy paper systems. These compounds have been found to provide excellent green-yellow colors when used in pressure sensitive carbonless copy-papers wherein the image is formed by the reaction of a color-forming compound with transition metal salts such as those of nickel, cobalt, iron, copper, and similar materials. These green-yellow color-formers have the advantage of greater solubility in encapsulation solvents and lower volatility than previously used yellow color-formers. The invention also concerns the admixture of these certain color-formers with N-(monosubstituted)dithiooxamides and/or N,N'-(disubstituted)dithiooxamides to form images of various colors and preferably black images during the application of appropriate pressure to pressure sensitive imaging constructions such as carbonless paper constructions.