• 1. An amorphous carbon nitride/NiO/CoN-based composite: a highly efficient nonprecious electrode for supercapacitors and the oxygen evolution reaction?
  Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
• 2. Aggregation-induced emission enhancement in halochalcones?
  Patricia A. A. M. Vaz,Jo?o Rocha,Artur M. S. Silva New J. Chem., 2016,40, 8198-8201
• 3. Aggregation of biologically important peptides and proteins: inhibition or acceleration depending on protein and metal ion concentrations
  Benjamin Gabriel Poulson,Kacper Szczepski,Joanna Izabela Lachowicz,Lukasz Jaremko,Abdul-Hamid Emwas,Mariusz Jaremko RSC Adv., 2020,10, 215-227
• 4. An analysis of the WTC fires using CIB correlations and simple modeling
  JGQuintiere
• 5. An anti-ultrasonic-stripping effect in confined micro/nanoscale cavities and its applications for efficient multiscale metallic patterning?
  Quan Xiang,Yiqin Chen,Zhiqin Li,Kaixi Bi,Guanhua Zhang,Huigao Duan Nanoscale, 2016,8, 19541-19550

• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers Anisoles

4-(4-Methoxyphenyl)-3-buten-2-one (CAS No. 943-88-4): A Comprehensive Overview

4-(4-Methoxyphenyl)-3-buten-2-one, also known by its CAS number 943-88-4, is a versatile organic compound that has garnered significant attention in the fields of organic synthesis, medicinal chemistry, and pharmaceutical research. This compound is characterized by its unique structure, which includes a methoxyphenyl substituent and a butenone moiety, making it an interesting candidate for various applications.

The chemical formula of 4-(4-methoxyphenyl)-3-buten-2-one is C₁₀H₁₂O₂, and it has a molecular weight of 164.20 g/mol. The compound is a colorless to pale yellow liquid with a characteristic odor. Its physical and chemical properties, such as solubility in organic solvents and reactivity, make it suitable for use in a wide range of synthetic reactions and as a building block in the development of new compounds.

In the realm of organic synthesis, 4-(4-methoxyphenyl)-3-buten-2-one serves as a valuable intermediate due to its reactivity and functional group versatility. The methoxyphenyl group can undergo various transformations, such as demethylation to form phenols or substitution reactions to introduce different substituents. The butenone moiety can participate in Michael additions, aldol condensations, and other carbon-carbon bond-forming reactions, making it an essential component in the synthesis of complex molecules.

Recent studies have highlighted the potential of 4-(4-methoxyphenyl)-3-buten-2-one in medicinal chemistry and drug discovery. One notable application is its use as a precursor in the synthesis of bioactive compounds with therapeutic potential. For instance, researchers have explored its role in the development of anti-inflammatory agents, where the compound's ability to modulate specific biological pathways has shown promising results.

In the context of pharmaceutical research, 4-(4-methoxyphenyl)-3-buten-2-one has been investigated for its potential as a lead compound in the development of new drugs. Its structural features allow for the introduction of various functional groups that can enhance its pharmacological properties. For example, modifications to the methoxyphenyl group have been shown to improve the compound's binding affinity to specific receptors, thereby enhancing its therapeutic efficacy.

The safety and toxicity profile of 4-(4-methoxyphenyl)-3-buten-2-one have also been evaluated in several studies. While it is generally considered safe for use in laboratory settings, proper handling and storage practices are essential to ensure safety. Researchers should adhere to standard laboratory protocols and use appropriate personal protective equipment (PPE) when working with this compound.

In addition to its applications in organic synthesis and pharmaceutical research, 4-(4-methoxyphenyl)-3-buten-2-one has found use in other areas such as materials science and analytical chemistry. Its unique properties make it suitable for use as a reference standard in chromatographic analyses and as a component in polymer formulations.

The ongoing research into 4-(4-methoxyphenyl)-3-buten-2-one continues to uncover new applications and potential uses. As scientists delve deeper into its chemical behavior and biological activity, this compound is likely to play an increasingly important role in various scientific disciplines.

In conclusion, 4-(4-methoxyphenyl)-3-buten-2-one (CAS No. 943-88-4) is a multifaceted compound with significant potential in multiple fields. Its unique structure and versatile properties make it an invaluable tool for researchers working in organic synthesis, medicinal chemistry, pharmaceutical development, and beyond. As research continues to advance, the applications of this compound are expected to expand further, contributing to scientific progress and innovation.

• 56600-90-9(4-(6-Methoxy-2-naphthyl)-3-buten-2-one)
• 62643-62-3(1,4-Pentadien-3-one, 1-[1,1'-biphenyl]-4-yl-5-(4-methoxyphenyl)-)
• 62643-60-1(1,4-Pentadien-3-one, 1-(4-methoxyphenyl)-5-(4-methylphenyl)-)
• 62378-72-7(3,5-Hexadien-2-one, 6-(4-methoxyphenyl)-)
• 37951-12-5((1E,4E)-1,5-Bis(4-methoxyphenyl)penta-1,4-dien-3-one)
• 3815-30-3(4-(4-Methoxyphenyl)-3-buten-2-one)
• 2051-07-2(1,5-Bis-(4-methoxyphenyl)-3-pentadienone)
• 104-27-8(a-Methylanisalacetone)
• 20766-31-8(4-(3-methoxyphenyl)but-3-en-2-one)
• 30625-53-7(3-Buten-2-one,4-(3-methoxyphenyl)-, (3E)-)