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1-(3-Ethoxy-4-Methoxyphenyl)-2-(Methylsulfonyl) ethanone CAS:1450657-28-9

1-(3-Ethoxy-4-Methoxyphenyl)-2-(Methylsulfonyl)ethanone is a chemical compound recognized for its diverse applications in organic synthesis and medicinal chemistry. Synthesized through the reaction of 3-ethoxy-4-methoxybenzoyl chloride with dimethyl sulfone, this compound exhibits distinctive structural features that contribute to its functional versatility and potential pharmacological activities.


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Application and Effect:

The structural characteristics of 1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethanone are significant: Aryl Ketone Core: Central to its structure is an aryl ketone motif, comprising a phenyl ring substituted with both ethoxy and methoxy groups, conferring electronic properties conducive to various chemical interactions. Methylsulfonyl Group: Attached to the ethanone backbone, the methylsulfonyl moiety enhances the compound's reactivity and influences its potential biological activities. Ether and Ester Functionalities: Presence of ethoxy and methoxy substituents introduces flexibility and potential for hydrogen bonding, crucial for biological interactions. Steric Effects: Substitution pattern around the phenyl ring affects molecular shape and can impact binding affinity and selectivity. Chemical Applications 1-(3-Ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethanone demonstrates broad chemical utility: Medicinal Chemistry: Used as a building block for designing analogs with potential pharmaceutical applications, targeting specific biological pathways. Synthetic Intermediacy: Acts as an intermediate in the synthesis of more complex molecules, including pharmaceuticals and agrochemicals. Functional Group Diversity: Ether and methoxy groups contribute to solubility and pharmacokinetic properties, influencing drug delivery and efficacy. Pharmacological Potential Research into its pharmacological properties highlights several potential avenues: Antimicrobial Activity: Structural components suggest potential antimicrobial properties, warranting investigation against various pathogens. Anti-inflammatory Effects: Ether and methoxy groups may contribute to anti-inflammatory properties, relevant in treating inflammatory conditions. Enzyme Inhibition: Methylsulfonyl group's presence suggests potential for enzyme inhibition, impacting metabolic pathways and disease states. Future Directions Future research directions for 1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethanone include: Structure-Activity Relationships: Further exploring how structural modifications affect its biological activity and optimizing derivatives for enhanced efficacy. Drug Design: Utilizing its multifunctional groups to develop novel therapeutics targeting specific diseases or biological mechanisms. Toxicological Studies: Assessing its safety profile and potential side effects to ensure suitability for clinical applications. Conclusion In conclusion, 1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethanone is a versatile compound pivotal in organic synthesis and medicinal chemistry. Its unique structural attributes and functional diversity underscore its potential in drug discovery and development, offering opportunities for creating new pharmaceuticals with tailored pharmacological properties. Ongoing research into its synthesis methodologies and pharmacological effects promises to unveil further applications in healthcare and related fields, solidifying its significance in modern chemical research and therapeutic innovation.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C12H16O5S
Assay 99%
Appearance white powder
CAS No.  1450657-28-9
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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