96919-48-1 Usage
Description
3-(2-NITRO-PHENYL)-THIOPHENE is a heterocyclic aromatic compound that features a thiophene ring with a nitrophenyl group attached at the third position. This unique structure endows it with distinctive electronic and structural properties, making it a valuable building block in organic synthesis and material science. Its reactivity, stemming from the nitro group, and the inherent characteristics of the thiophene ring, position this compound as a promising candidate for the development of innovative materials and organic molecules.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 96919-48-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,9,1 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96919-48:
(7*9)+(6*6)+(5*9)+(4*1)+(3*9)+(2*4)+(1*8)=191
191 % 10 = 1
So 96919-48-1 is a valid CAS Registry Number.
96919-48-1Relevant articles and documents
Thieno[2,3-b]indole-Based Small Push-Pull Chromophores: Synthesis, Structure, and Electronic Properties
Baert, Fran?ois,Cabanetos, Clément,Allain, Magali,Silvestre, Virginie,Leriche, Philippe,Blanchard, Philippe
, p. 1582 - 1585 (2016)
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
Mo–Catalyzed One-Pot Synthesis of N-Polyheterocycles from Nitroarenes and Glycols with Recycling of the Waste Reduction Byproduct. Substituent-Tuned Photophysical Properties
Hernández-Ruiz, Raquel,Rubio-Presa, Rubén,Suárez-Pantiga, Samuel,Pedrosa, María R.,Fernández-Rodríguez, Manuel A.,Tapia, M. José,Sanz, Roberto
supporting information, p. 13613 - 13623 (2021/08/23)
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.
TRICYCLIC CRBN LIGANDS AND USES THEREOF
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Paragraph 0764; 0765, (2020/01/24)
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.
