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• Solvents and Organic Chemicals Organic Compounds Aldehyde/Ketone

Introduction to 2-(4-Formylphenoxy)acetic Acid (CAS No. 22042-71-3)

2-(4-Formylphenoxy)acetic Acid (CAS No. 22042-71-3) is a versatile organic compound that has garnered significant attention in the fields of chemistry, biology, and pharmaceutical research. This compound, also known as 4-formylphenoxyacetic acid, is characterized by its unique structure and functional groups, which make it a valuable intermediate in the synthesis of various pharmaceuticals and fine chemicals.

The molecular formula of 2-(4-Formylphenoxy)acetic Acid is C₉H₈O₃, and its molecular weight is 164.16 g/mol. The compound features a carboxylic acid group (-COOH) and an aldehyde group (-CHO), both of which are attached to a phenyl ring through an ether linkage. This combination of functional groups imparts distinct chemical properties and reactivity, making it a useful building block in organic synthesis.

In recent years, 2-(4-Formylphenoxy)acetic Acid has been extensively studied for its potential applications in the development of new drugs and therapeutic agents. One notable area of research involves its use as a precursor in the synthesis of antiviral compounds. For instance, a study published in the Journal of Medicinal Chemistry highlighted the role of 2-(4-Formylphenoxy)acetic Acid in the synthesis of novel antiviral agents targeting RNA-dependent RNA polymerases, which are crucial enzymes in viral replication processes.

Beyond antiviral applications, 2-(4-Formylphenoxy)acetic Acid has also shown promise in the field of cancer research. A recent study published in the European Journal of Medicinal Chemistry demonstrated that derivatives of this compound exhibit potent cytotoxic activity against various cancer cell lines. The researchers found that these derivatives can effectively inhibit cell proliferation and induce apoptosis, suggesting their potential as lead compounds for the development of new anticancer drugs.

The versatility of 2-(4-Formylphenoxy)acetic Acid extends to its use as a ligand in coordination chemistry. Its ability to form stable complexes with metal ions has been explored for various applications, including catalysis and materials science. For example, a study published in Inorganic Chemistry reported the synthesis and characterization of metal complexes derived from 2-(4-Formylphenoxy)acetic Acid. These complexes exhibited excellent catalytic activity in the oxidation of alcohols and other organic substrates, highlighting their potential in industrial processes.

In addition to its synthetic applications, 2-(4-Formylphenoxy)acetic Acid has been investigated for its biological activities. Research has shown that this compound can modulate various signaling pathways involved in inflammation and oxidative stress. A study published in Bioorganic & Medicinal Chemistry Letters reported that derivatives of 2-(4-Formylphenoxy)acetic Acid can effectively inhibit the production of pro-inflammatory cytokines and reactive oxygen species (ROS), suggesting their potential as anti-inflammatory agents.

The safety profile of 2-(4-Formylphenoxy)acetic Acid is another important aspect that has been studied extensively. Toxicological evaluations have indicated that this compound is generally well-tolerated at low concentrations, with minimal adverse effects observed in animal models. However, as with any chemical compound, proper handling and storage precautions should be followed to ensure safety.

In conclusion, 2-(4-Formylphenoxy)acetic Acid (CAS No. 22042-71-3) is a multifunctional compound with a wide range of applications in pharmaceuticals, fine chemicals, and materials science. Its unique chemical structure and reactivity make it an invaluable intermediate in the synthesis of novel compounds with diverse biological activities. Ongoing research continues to uncover new possibilities for this compound, further solidifying its importance in modern scientific endeavors.

• 6280-80-4(2-(2-Formylphenoxy)acetic acid)
• 1643-15-8(2-(3-methylphenoxy)acetic acid)
• 51264-68-7(Ethyl (3-formylphenoxy)acetate)
• 940-64-7(2-(4-methylphenoxy)acetic acid)
• 37748-10-0(Methyl (3-formylphenoxy)acetate)
• 1660-19-1((4-Formyl-2-methoxyphenoxy)acetic Acid)
• 19360-67-9(4-H2CPA)
• 5406-14-4((3,5-Dimethylphenoxy)acetic Acid)
• 643074-77-5(1,3-Benzenedicarboxylic acid, 5-(carboxymethoxy)-)
• 64038-41-1(Acetic acid,2-(2-formylphenoxy)-, sodium salt (1:1))