925674-54-0

Basic information

• Product Name: Thieno[3,4-b]-1,4-dioxin, 2,3-dihydro-5-(4-methoxyphenyl)-
• Synonyms: Thieno[3,4-b]-1,4-dioxin, 2,3-dihydro-5-(4-methoxyphenyl)-
• CAS NO: 925674-54-0
• Molecular Formula: C₁₃H₁₂O₃S
• Molecular Weight: 248.30
• Mol File: 925674-54-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Thieno[3,4-b]-1,4-dioxin, 2,3-dihydro-5-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Thieno[3,4-b]-1,4-dioxin, 2,3-dihydro-5-(4-methoxyphenyl)-(925674-54-0)
• EPA Substance Registry System: Thieno[3,4-b]-1,4-dioxin, 2,3-dihydro-5-(4-methoxyphenyl)-(925674-54-0)

Safety Data

• Hazardous Substances Data: 925674-54-0(Hazardous Substances Data)

Usage

Description

Thieno[3,4-b]-1,4-dioxin, 2,3-dihydro-5-(4-methoxyphenyl)is a chemical compound characterized by a thieno ring fused to a dioxin ring, along with a dihydro group connected to a 4-methoxyphenyl moiety. This unique molecular structure endows it with potential biological and pharmacological activities, making it a promising candidate in research and pharmaceutical development.

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 articles and documents

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

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.