925674-54-0

Usage

Uses

Used in Pharmaceutical Development:
Thieno[3,4-b]-1,4-dioxin, 2,3-dihydro-5-(4-methoxyphenyl)is utilized as a pharmaceutical agent for its potential anti-cancer properties. Its unique chemical structure allows it to interact with various biological targets, making it a valuable molecule in the discovery and development of new drugs for cancer treatment.
Used in Neurobiological Research:
In the field of neurobiology, Thieno[3,4-b]-1,4-dioxin, 2,3-dihydro-5-(4-methoxyphenyl)is employed as a research tool to study its ability to modulate neurobiological receptors and pathways. This can lead to a better understanding of its potential applications in treating neurological disorders and developing new therapeutic strategies.
Used in Drug Discovery:
Due to its diverse interactions with biological targets, Thieno[3,4-b]-1,4-dioxin, 2,3-dihydro-5-(4-methoxyphenyl)is also used in drug discovery processes. Its unique structure makes it a valuable compound for exploring new therapeutic avenues and identifying potential drug candidates for various diseases and conditions.

Upstream product

• 696-62-8 para-iodoanisole 
• 126213-50-1 3,4-(ethylenedioxy)thiophene 
• 250726-93-3 2-(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-4,4,5,5-tetramethyl-2-thiophen-2-yl-1,3,2-dioxaborolane 
• 852054-42-3 7-bromo-2,3-dihydrothieno[3,4-b][1,4]dioxine-5-carbaldehyde 
• 925674-70-0 2,3-dihydro-7-(4-methoxyphenyl)thieno[3,4-b][1,4]dioxine-5-carbaldehyde 
• 1031685-80-9 5-(4-methoxyphenyl)-3,4-ethylenedioxythenyl alcohol 
• 104-92-7 1-bromo-4-methoxy-benzene 

Downstream Products

• 925674-70-0 2,3-dihydro-7-(4-methoxyphenyl)thieno[3,4-b][1,4]dioxine-5-carbaldehyde 

Relevant academic research and scientific papers

Efficient synthesis of mono- and bis-arylated ethylenedioxy thiophene-based functional π-conjugated molecules via clay-supported palladium-catalysed direct arylation reactions

An active Pd catalyst was prepared by the modification of montmorillonite clay. The catalyst was found to be effective for the synthesis of ethylenedioxy thiophene-based π-conjugated molecules. The reaction proceeded through clay-supported Pd-catalysed di

Metal-Free Aerobic Oxidative Selective C-C Bond Cleavage in Heteroaryl-Containing Primary and Secondary Alcohols

A transition-metal-free aerobic oxidative selective C-C bond-cleavage reaction in primary and secondary heteroaryl alcohols is reported. This reaction was highly efficient and tolerated various heteroaryl alcohols, generating a carboxylic acid derivative and a neutral heteroaromatic compound. Experimental studies combined with density functional theory calculations revealed the mechanism underlying the selective C-C bond cleavage. This strategy also provides an alternative simple approach to carboxylation reaction.

Synthesis of mono- and bis-arylated 3,4-(ethylenedioxythiophenes) via direct palladium catalyzed arylation reactions

The synthesis of arylated/heteroarylated 3,4-ethylenedioxythiophene derivatives is reported using a straightforward palladium mediated Heck coupling of 3,4-ethylenedioxythiophene with various aryl/heteroaryl halides.

Pd-mediated C-H arylation of EDOT and synthesis of push-pull systems incorporating EDOT

The direct C-H arylation of 3,4-ethylenedioxythiophene (EDOT) is described under Heck-type experimental conditions. This methodology has been used to synthesize a series of push-pull systems containing EDOT units.