1185916-56-6

Basic information

• Product Name: 3-(5-Fluoro-2,4-dinitrophenyl)thiophene
• Synonyms: 3-(5-fluoro-2,4-dinitrophenyl)thiophene;1185916-56-6;CHEMBL2229893
• CAS NO: 1185916-56-6
• Molecular Weight: 268.225
• Mol File: 1185916-56-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(5-Fluoro-2,4-dinitrophenyl)thiophene(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(5-Fluoro-2,4-dinitrophenyl)thiophene(1185916-56-6)
• EPA Substance Registry System: 3-(5-Fluoro-2,4-dinitrophenyl)thiophene(1185916-56-6)

Safety Data

• Hazardous Substances Data: 1185916-56-6(Hazardous Substances Data)

Usage

General Description

3-(5-Fluoro-2,4-dinitrophenyl)thiophene is a chemical compound that contains a thiophene ring with a 5-fluoro-2,4-dinitrophenyl group attached. It is often used in organic synthesis and pharmaceutical research due to its potential pharmacological properties. The presence of the fluoro and dinitro groups on the phenyl ring makes this compound highly reactive and can be used as a reagent in various chemical reactions. It has also been studied for its potential applications in the field of material science, such as in the development of electronic and optoelectronic devices. Overall, 3-(5-Fluoro-2,4-dinitrophenyl)thiophene is a versatile compound with applications in both organic chemistry and material science.

Upstream product

• 872-31-1 3-Bromothiophene 
• 400-91-9 1-bromo-3-fluoro-4,6-dinitrobenzene 

Downstream Products

• 1185916-64-6 C₁₀H₄FN₃O₆S 
• 1185916-71-5 C₁₀H₄FN₃O₆S 

Relevant articles and documents

Design, synthesis, and fungicidal activity of novel analogues of pyrrolnitrin

A series of novel analogues of pyrrolnitrin containing a thiophene moiety were designed and synthesized by a facile method, and their structures were characterized by 1H nuclear magnetic resonance (NMR) and high-resolution mass spectrometry. The isomers IV-h and V-h were isolated, and their structures were identified by 2D NMR, including heteronuclear multiple-quantum coherence (HMQC), heteronuclear multiple-bond correlation (HMBC), and nuclear Overhauser effect spectrometry (NOESY) spectra. Their fungicidal activities against five fungi were evaluated, and the results indicated that some of the title compounds showed excellent fungicidal activities in vitro against Alternaria solani, Gibberella zeae, Physalospora piricola, Fusarium omysporum, and Cercospora arachidicola at the dosage of 50 μg mL-1. Some compounds shown moderate activity at low dosage. Compound V-h could be considered as a leading structure for further design of agricultural fungicides.