152920-53-1

Basic information

• Product Name: 5-(3-THIENYL)-1H-INDOLE
• Synonyms: 5-THIOPHEN-3-YL-1H-INDOLE;AKOS BAR-1294;5-(3-THIENYL)-1H-INDOLE;1H-Indole,5-(3-thienyl)-
• CAS NO: 152920-53-1
• Molecular Formula: C₁₂H₉NS
• Molecular Weight: 199.27
• Mol File: 152920-53-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-(3-THIENYL)-1H-INDOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(3-THIENYL)-1H-INDOLE(152920-53-1)
• EPA Substance Registry System: 5-(3-THIENYL)-1H-INDOLE(152920-53-1)

Safety Data

• Hazardous Substances Data: 152920-53-1(Hazardous Substances Data)

Usage

General Description

5-(3-thienyl)-1H-indole, also known as 3-thienylindole, is a chemical compound with the molecular formula C12H9NS. It is a heterocyclic compound that contains both a thienyl and an indole ring. This chemical has been studied for its potential use in organic light-emitting diodes (OLEDs) and as a possible pharmaceutical compound. It has been shown to have anti-inflammatory and anticancer properties, making it a potential candidate for the development of new drugs. Additionally, 5-(3-thienyl)-1H-indole has been investigated for its potential use in the synthesis of novel organic materials and polymers. Overall, this compound has shown promise in various fields and has the potential to be further explored for its diverse applications.

Upstream product

• 872-31-1 3-Bromothiophene 
• 144104-59-6 1H-indole-5-boronic acid 
• 10075-50-0 5-bromo-1H-indole 
• 6165-69-1 Thien-3-ylboronic acid 
• 17249-80-8 3-chlorothiophene 
• 17422-32-1 5-chloro-1H-indole 

Relevant articles and documents

Highly efficient monophosphine-based catalyst for the palladium-catalyzed Suzuki-Miyaura reaction of heteroaryl halides and heteroaryl boronic acids and esters

A highly active and efficient catalyst system derived from a palladium precatalyst and monophosphine ligands 1 or 2 for the Suzuki-Miyaura cross-coupling reaction of heteroaryl boronic acids and esters has been developed. This method allows for the preparation of a wide variety of heterobiaryls in good to excellent yields and displays a high level of activity for the coupling of heteroaryl chlorides as well as hindered aryl and heteroaryl halides. Specific factors that govern the efficacy of the transformation for certain heterocyclic motifs were also investigated.

Conjugated oligomers with thiophene and indole moieties: Synthesis, photoluminescence and electrochromic performances

Two series of thiophene oligomers and terthiophene oligomers consisting of both thiophene and indole moieties have been synthesized. They have same excitation-dependent photoluminescence characteristics, but different bandgaps and absorption behaviors, which relates to the number and denseness of indoles in the conjugated oligomers and the length of alkyl chains on indole moiety due to varied the π-π stacking interaction of conjugated structures in the as-prepared oligomers. A simple electrochromic device based on such a conjugated oligomer displays a novel four-color electrochromism from red to yellow, green and puce with the increased potential and possesses good environmental and redox stability. Such conjugated oligomer also exhibits high sensitivity and selectivity for Zn2+detection.