166904-09-2

Usage

General Description

3-methoxy-4-(4-nitrophenoxy)benzaldehyde is a chemical compound that consists of a benzaldehyde group substituted with a methoxy group at the 3-position and a 4-(4-nitrophenoxy) group at the 4-position. 3-methoxy-4-(4-nitrophenoxy)benzaldehyde is commonly used in organic synthesis and pharmaceutical research. It has potential applications in the development of novel drugs and as an intermediate in the production of various aromatic compounds. The presence of a nitro group in the molecule makes it useful in the synthesis of complex organic molecules and as a building block for pharmaceutical compounds. Additionally, the methoxy group contributes to the compound's reactivity and can enhance its solubility in various solvents. Overall, 3-methoxy-4-(4-nitrophenoxy)benzaldehyde is a versatile chemical with a wide range of potential applications in the field of chemistry and pharmaceuticals.

Upstream product

• 121-33-5 vanillin 
• 350-46-9 4-Fluoronitrobenzene 
• 100-00-5 4-chlorobenzonitrile 

Downstream Products

• 875246-01-8 3-methoxy-4-phenoxybenzoic acid 
• 129623-63-8 3-hydroxy-4-phenoxy-benzoic acid 
• 4664-65-7 3-methoxy-4-phenoxybenzyl alcohol 
• 4664-62-4 3-methoxy-4-benzoxybenzaldehyde 
• 35065-13-5 3-hydroxy-4-phenoxybenzaldehyde 
• 916793-29-8 (3-methoxy-4-(4-nitrophenoxy)phenyl)methanol 

Relevant academic research and scientific papers

GLUCOCORTICOID RECEPTOR AGONIST AND IMMUNOCONJUGATES THEREOF

Provided herein are glucocorticoid receptor agonist immunoconjugates, glucocorticoid receptor agonists, and methods of using the same, e.g., to treat autoimmune or inflammatory diseases.

Design of mechanism-based inhibitors of transthyretin amyloidosis: Studies with biphenyl ethers and new structural templates

Transthyretin (TTR), a tetrameric thyroxine (T4) carrier protein, is associated with a variety of amyloid diseases. In this study, we explore the potential of biphenyl ethers (BPE), which are shown to interact with a high affinity to its T4 binding site t

Novel diphenyl ethers: Design, docking studies, synthesis and inhibition of enoyl ACP reductase of Plasmodium falciparum and Escherichia coli

We designed some novel diphenyl ethers and determined their binding energies for Enoyl-Acyl Carrier Protein Reductase (ENR) of Plasmodium falciparum using Autodock. Out of these, we synthesized the promising compounds and tested them for their inhibitory

Synthesis and insecticidal activity of new substituted phenoxychalcones

Substituted acetophenones (1a-d) on condensation with substituted phenoxyaldehydes (2a-d) in the presence of KOH (50percent) and ethanol give new substituted phenoxychalcones (3a-l).Compounds 3b and 3e have been found to be insecticidally active against housefly (Musca domestica nebulo) adults.