• 1. Metabolic engineering for plant natural products biosynthesis: new procedures, concrete achievements and remaining limits
  Vincent Courdavault,Sarah E. O'Connor,Michael K. Jensen,Nicolas Papon Nat. Prod. Rep. 2021 38 2145
• 2. Recent trends in biocatalysis
  Dong Yi,Thomas Bayer,Christoffel P. S. Badenhorst,Shuke Wu,Mark Doerr,Matthias H?hne,Uwe T. Bornscheuer Chem. Soc. Rev. 2021 50 8003

• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenols 1-hydroxy-2-unsubstituted benzenoids

3-(4-Hydroxyphenyl)Propanal (CAS No. 20238-83-9): A Comprehensive Overview

3-(4-Hydroxyphenyl)Propanal, also known by its CAS registry number 20238-83-9, is a versatile organic compound that has garnered significant attention in both academic and industrial research. This compound, characterized by its aromatic ring and aldehyde functional group, exhibits unique chemical properties that make it valuable in various applications. Recent advancements in synthetic chemistry and material science have further highlighted its potential in drug development, food additives, and specialty chemicals.

The molecular structure of 3-(4-Hydroxyphenyl)Propanal consists of a benzene ring substituted with a hydroxyl group at the para position and a propanal chain. This arrangement imparts the compound with antioxidant properties, which have been extensively studied in recent years. Researchers have found that the compound's ability to scavenge free radicals makes it a promising candidate for use in cosmetic formulations and pharmaceuticals aimed at combating oxidative stress.

One of the most notable recent developments involving 3-(4-Hydroxyphenyl)Propanal is its application in the synthesis of advanced materials. Scientists have successfully utilized this compound as a precursor for the creation of polymeric materials with enhanced thermal stability and mechanical properties. These materials are being explored for use in high-performance electronics and aerospace applications, where durability under extreme conditions is critical.

In the field of food science, 3-(4-Hydroxyphenyl)Propanal has been investigated for its role as a natural flavor enhancer. Studies have demonstrated that the compound can impart a desirable aromatic profile to food products, making it a potential alternative to artificial flavoring agents. This aligns with the growing consumer demand for natural and sustainable food additives.

The synthesis of 3-(4-Hydroxyphenyl)Propanal has also seen significant improvements. Traditional methods often involved multi-step processes with low yields, but recent innovations have introduced more efficient routes. For instance, researchers have developed catalytic systems that enable the direct oxidation of alcohols to aldehydes under mild conditions, significantly streamlining the production process.

From a pharmacological perspective, 3-(4-Hydroxyphenyl)Propanal has shown potential as a lead compound in drug discovery. Its ability to interact with specific biological pathways has been explored in preclinical studies targeting inflammatory diseases and neurodegenerative disorders. While further research is needed to establish its efficacy in clinical settings, these findings underscore its importance as a tool in medicinal chemistry.

In conclusion, 3-(4-Hydroxyphenyl)Propanal (CAS No. 20238-83-9) is a multifaceted compound with applications spanning multiple industries. Its unique chemical properties, combined with recent advancements in synthesis and application techniques, position it as a key player in modern material science and pharmaceutical research. As ongoing studies continue to uncover new uses for this compound, its significance in both academic and industrial settings is likely to grow further.

• 770-39-8(4-Hydroxyphenylacetone)
• 169334-30-9(2-Hexanone, 6-(4-hydroxyphenyl)-)
• 113482-94-3(3,5-Heptanedione,1,7-bis(4-hydroxyphenyl)-)
• 545442-98-6(3-(3,4-dihydroxyphenyl)propanal)
• 5471-51-2(Raspberry ketone)
• 93652-23-4(3-Pentanone, 1,5-bis(4-hydroxyphenyl)-)
• 26172-10-1(3-(3-Hydroxy-phenyl)-propionaldehyde)
• 182219-43-8(4-(4’-Hydroxyphenyl)-2-butanone-d5)
• 130233-83-9(3-Heptanone,1,7-bis(4-hydroxyphenyl)-)
• 139446-84-7(3-Decanone, 1-(4-hydroxyphenyl)-)