96919-48-1

Basic information

• Product Name: 3-(2-NITRO-PHENYL)-THIOPHENE
• Synonyms: 3-(2-NITRO-PHENYL)-THIOPHENE;3-(o-nitrophenyl)thiophene
• CAS NO: 96919-48-1
• Molecular Formula: C₁₀H₇NO₂S
• Molecular Weight: 205.23
• Mol File: 96919-48-1.mol
• Article Data: 17

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(2-NITRO-PHENYL)-THIOPHENE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-NITRO-PHENYL)-THIOPHENE(96919-48-1)
• EPA Substance Registry System: 3-(2-NITRO-PHENYL)-THIOPHENE(96919-48-1)

Safety Data

• Hazardous Substances Data: 96919-48-1(Hazardous Substances Data)

Usage

General Description

3-(2-Nitro-phenyl)-thiophene is a chemical compound consisting of a thiophene ring with a nitrophenyl group attached at the third position. It is a heterocyclic aromatic compound with potential applications in the field of organic synthesis and material science. The presence of the nitro group makes this compound reactive and useful as a building block for the synthesis of various other organic molecules. Additionally, the thiophene ring provides unique electronic and structural properties, making it suitable for the development of functional materials, such as organic semiconductors and optoelectronic devices. The combination of the nitrophenyl and thiophene moieties in this compound could provide opportunities for the development of novel compounds with enhanced properties for various applications.

Upstream product

• 872-31-1 3-Bromothiophene 
• 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 
• 98-80-6 phenylboronic acid 
• 5570-19-4 2-nitrophenylboronic acid 
• 10486-61-0 3-thienyl iodide 

Downstream Products

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

Relevant articles and documents

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

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.

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.