96919-48-1

Usage

Uses

Used in Organic Synthesis:
3-(2-NITRO-PHENYL)-THIOPHENE is used as a reactive intermediate for the synthesis of a variety of organic molecules. Its nitro group allows for further chemical reactions, making it a versatile component in creating complex organic compounds.
Used in Material Science:
In the field of material science, 3-(2-NITRO-PHENYL)-THIOPHENE is utilized as a key component in the development of functional materials. Its unique electronic properties contribute to the creation of advanced materials with specific applications.
Used in the Development of Organic Semiconductors:
3-(2-NITRO-PHENYL)-THIOPHENE is used as a building block in the synthesis of organic semiconductors. The combination of the nitrophenyl and thiophene moieties provides opportunities to engineer materials with tailored electronic properties, suitable for use in electronic devices and circuits.
Used in Optoelectronic Devices:
3-(2-NITRO-PHENYL)-THIOPHENE is also used in the development of optoelectronic devices, where its structural and electronic characteristics can be leveraged to enhance the performance of devices such as solar cells, light-emitting diodes (LEDs), and photodetectors.
Used in Pharmaceutical Industry:
3-(2-NITRO-PHENYL)-THIOPHENE may be employed as a starting material for the synthesis of pharmaceutical compounds, given its reactivity and the potential for creating diverse molecular structures with therapeutic properties.
Used in Chemical Research:
In academic and industrial research settings, 3-(2-NITRO-PHENYL)-THIOPHENE serves as a subject of study for understanding the properties and reactions of heterocyclic compounds, contributing to the advancement of chemical knowledge and technology.

Upstream product

• 10486-61-0 3-thienyl iodide 
• 577-19-5 2-nitrophenyl bromide 
• 188290-36-0 thiophene 
• 88-74-4 2-nitro-aniline 
• 6165-69-1 Thien-3-ylboronic acid 
• 609-73-4 o-nitroiodobenzene 
• 872-31-1 3-Bromothiophene 
• 98-80-6 phenylboronic acid 
• 5570-19-4 2-nitrophenylboronic acid 

Downstream Products

• 96919-49-2 3-(o-aminophenyl)thiophene 
• 1185916-57-7 C₁₀H₆N₂O₄S 
• 18132-97-3 C₁₀H₆N₂O₄S 
• 1329603-61-3 C₄₄H₃₁N₃SSi 
• 1329603-48-6 C₂₆H₁₇N₃S 
• 1329604-09-2 C₁₆H₁₀BrNS 
• 1329604-10-5 C₁₆H₁₂BNO₂S 

Relevant academic research and scientific papers

Thieno[2,3-b]indole-Based Small Push-Pull Chromophores: Synthesis, Structure, and Electronic Properties

Small push-pull molecules were synthesized in high yields by connecting a N-methyl or N-phenyl substituted thieno[2,3-b]indole electron-donating block directly to a 2,2-dicyanovinyl or (1-(dicyanomethylene)-3-oxo-1-inden-2-ylidene)methyl electron-withdraw

COMPOUND AND PHOTOELECTRIC DEVICE, IMAGE SENSOR AND ELECTRONIC DEVICE INCLUDING THE SAME

A compound of Chemical Formula 1, and an organic photoelectric device, an image sensor, and an electronic device including the same are disclosed: In Chemical Formula 1, each substituent is the same as defined in the detailed description.

Mo–Catalyzed One-Pot Synthesis of N-Polyheterocycles from Nitroarenes and Glycols with Recycling of the Waste Reduction Byproduct. Substituent-Tuned Photophysical Properties

A catalytic domino reduction–imine formation–intramolecular cyclization–oxidation for the general synthesis of a wide variety of biologically relevant N-polyheterocycles, such as quinoxaline- and quinoline-fused derivatives, and phenanthridines, is reported. A simple, easily available, and environmentally friendly dioxomolybdenum(VI) complex has proven to be a highly efficient and versatile catalyst for transforming a broad range of starting nitroarenes involving several redox processes. Not only is this a sustainable, step-economical as well as air- and moisture-tolerant method, but also it is worth highlighting that the waste byproduct generated in the first step of the sequence is recycled and incorporated in the final target molecule, improving the overall synthetic efficiency. Moreover, selected indoloquinoxalines have been photophysically characterized in cyclohexane and toluene with exceptional fluorescence quantum yields above 0.7 for the alkyl derivatives.

Compound taking quinolinone derivative as core and application of compound in organic electroluminescent device

The invention discloses a compound taking a quinolinone derivative as a core and an application of the compound in an organic electroluminescent device. The compound structurally contains the quinolinone derivative as an electron acceptor, so that transmi

TRICYCLIC CRBN LIGANDS AND USES THEREOF

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of CRBN, and the treatment of CRBN-mediated disorders.

ORGANIC COMPOUND, ORGANIC ELECTRONIC DEVICE HAVING THE SAME, PHOTOELECTRIC CONVERSION ELEMENT HAVING THE SAME, IMAGING ELEMENT AND IMAGING DEVICE

PROBLEM TO BE SOLVED: To provide an organic compound having a high glass transition temperature, and an organic electronic device having the same. SOLUTION: The present invention provides an organic compound represented by formula [1] (R1-R10 independently represent H, halogen, cyano, alkyl, aryl, or heteroaryl; n is an integer of 0-2; m is an integer of 2-4; A is fluorene ring, benzofluorene ring, dibenzofluorene ring or spirofluorene ring; and B is C6-12 aryl or C4-11 heteroaryl). SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2019,JPOandINPIT

HETEROCYCLIC COMPOUND AND ORGANIC ELECTRONIC DEVICE COMPRISING THE SAME

The present specification relates to a heterocyclic compound represented by chemical formula 1 and an organic electronic device comprising the heterocyclic compound in an organic active layer. When the heterocyclic compound is used in the organic active l

IRIDIUM COMPLEX AND ORGANIC ELECTROLUMINESCENCE DEVICE USING THE SAME

The present invention discloses an iridium complex of formula (1) and an organic electroluminescence device employing the iridium complex as the phosphorescent dopant material. The organic EL device can display good performance, such as lower driving volt

Delay fluorescent compound and organic electroluminescence device employing same

The invention discloses a compound used as organic electroluminescence material. The compound has a structure indicated in formula (1) and the compound has good performance when serving as the delay fluorescent material of a light emitting layer or organi

Metal-free deoxygenation and reductive disilylation of nitroarenes by organosilicon reducing reagents

A metal-free deoxygenation and reductive disilylation of nitroarenes was achieved using N,N’-bis(trime-thylsilyl)-4,4’-bipyridinylidene (1) under mild and neutral reaction conditions, and a broad functional group tolerance was possible in this reaction. Mono-deoxygenation, giving a synthetically valuable N,O-bis(trimethylsilyl)phe-nylhydroxylamine (7a) as a readily available and safe phenylnitrene source from nitrobenzene, and double-deoxy-genation, giving N,N-bis(trimethylsilyl)anilines 8, were easily controlled by varying the amounts of 1 and reaction temperature as well as adding dibenzothiophene (DBTP). Reaction of 2-arylnitrobenzenes with 1 resulted in the formation of the corresponding carbazoles 14 via in situ-gen-erated phenylnitrene species derived by thermolysis of N,O-bis(trimethylsilyl)phenylhydroxylamines 7, followed by their subsequent intramolecular C H insertion. In addition, the intramolecular N N coupling reaction proceeded in the reduction of 2,2’-dinitrobiphenyl derivatives by 1, giving the corresponding benzo[c]cinnolines.