152920-53-1 Usage
Description
5-(3-THIENYL)-1H-INDOLE, also known as 3-thienylindole, is a heterocyclic chemical compound with the molecular formula C12H9NS. It features both a thienyl and an indole ring, which contribute to its unique properties and potential applications. 5-(3-THIENYL)-1H-INDOLE has been studied for its potential use in various fields, including organic light-emitting diodes (OLEDs), pharmaceutical development, and the synthesis of novel organic materials and polymers. Its anti-inflammatory and anticancer properties make it a promising candidate for the development of new drugs.
Uses
Used in Organic Light-Emitting Diodes (OLEDs):
5-(3-THIENYL)-1H-INDOLE is used as a component in the development of organic light-emitting diodes (OLEDs) for its ability to contribute to the emission of light in these devices, enhancing their performance and efficiency.
Used in Pharmaceutical Development:
5-(3-THIENYL)-1H-INDOLE is used as a potential pharmaceutical compound for its demonstrated anti-inflammatory and anticancer properties. It is being studied for its potential to be developed into new drugs that can treat various inflammatory conditions and cancer types.
Used in the Synthesis of Novel Organic Materials and Polymers:
5-(3-THIENYL)-1H-INDOLE is used as a building block in the synthesis of novel organic materials and polymers, where its unique structure and properties can contribute to the development of new materials with specific characteristics and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 152920-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,9,2 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 152920-53:
(8*1)+(7*5)+(6*2)+(5*9)+(4*2)+(3*0)+(2*5)+(1*3)=121
121 % 10 = 1
So 152920-53-1 is a valid CAS Registry Number.
152920-53-1Relevant articles and documents
Highly efficient monophosphine-based catalyst for the palladium-catalyzed Suzuki-Miyaura reaction of heteroaryl halides and heteroaryl boronic acids and esters
Billingsley, Kelvin,Buchwald, Stephen L.
, p. 3358 - 3366 (2007)
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
Dong, Ben,Li, Baoyan,Cao, Yi,Meng, Xinlei,Yan, Han,Ge, Shusheng,Lu, Yun
, p. 35 - 42 (2016/12/23)
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.
