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• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Carboxylic acid esters
• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Carboxylic acid derivatives Carboxylic acid esters
• Solvents and Organic Chemicals Organic Compounds Acids/Esters

Ethyl 3-Ethoxypropionate (CAS No. 763-69-9): A Comprehensive Overview

Ethyl 3-Ethoxypropionate (CAS No. 763-69-9) is a versatile organic compound that has gained significant attention in various fields, including chemical synthesis, pharmaceuticals, and materials science. This compound, also known as ethyl 3-ethoxypropanoate, is characterized by its unique chemical structure and favorable physical properties, making it a valuable reagent in numerous applications.

The molecular formula of Ethyl 3-Ethoxypropionate is C₇H₁₄O₃, and it has a molecular weight of approximately 146.18 g/mol. The compound is a colorless liquid with a mild, pleasant odor. It is soluble in most organic solvents and has a boiling point of around 155°C at atmospheric pressure. These properties make it suitable for use in a wide range of chemical processes and formulations.

In the realm of chemical synthesis, Ethyl 3-Ethoxypropionate serves as an important intermediate and solvent. Its reactivity and stability make it an ideal choice for various synthetic pathways, particularly in the preparation of complex organic molecules. Recent studies have highlighted its utility in the synthesis of pharmaceutical intermediates, where it can be used to introduce specific functional groups or to facilitate the formation of desired bonds.

One notable application of Ethyl 3-Ethoxypropionate is in the development of pharmaceuticals. Its ability to act as a solvent and reagent in drug synthesis has led to its use in the production of various medications. For instance, it has been employed in the synthesis of anti-inflammatory drugs, antiviral agents, and other therapeutic compounds. The compound's low toxicity and favorable safety profile further enhance its suitability for pharmaceutical applications.

In materials science, Ethyl 3-Ethoxypropionate has found applications in the formulation of coatings, adhesives, and polymers. Its ability to improve the solubility and compatibility of different components makes it an effective additive in these formulations. Recent research has explored its use in the development of environmentally friendly materials, where it can help reduce the environmental impact by replacing more hazardous solvents.

The environmental impact of Ethyl 3-Ethoxypropionate is another area of active research. Studies have shown that it has a relatively low environmental persistence and toxicity compared to many other organic solvents. This makes it a preferred choice for green chemistry initiatives aimed at reducing the ecological footprint of chemical processes.

In addition to its practical applications, Ethyl 3-Ethoxypropionate has been the subject of numerous academic studies aimed at understanding its fundamental properties and behavior. These studies have provided valuable insights into its reactivity, stability, and interactions with other chemicals. For example, recent research has explored its use as a model compound for studying solvent effects on reaction kinetics and mechanisms.

The safety profile of Ethyl 3-Ethoxypropionate is well-documented. It is generally considered to be non-toxic and non-irritating when handled properly. However, like any chemical compound, it should be used with appropriate safety measures to prevent accidental exposure or misuse. Proper handling guidelines and storage conditions are essential to ensure its safe use in both laboratory and industrial settings.

In conclusion, Ethyl 3-Ethoxypropionate (CAS No. 763-69-9) is a multifaceted compound with a wide range of applications in chemical synthesis, pharmaceuticals, materials science, and environmental chemistry. Its unique properties and favorable safety profile make it an invaluable reagent in various fields. Ongoing research continues to uncover new uses and potential benefits of this compound, further solidifying its importance in modern chemistry.

• 14144-41-3(Propanoic acid,3-propoxy-, propyl ester)
• 623-72-3(Ethyl 3-hydroxypropanoate)
• 886362-92-1(3-3-(2-Ethoxycarbonylethoxy)propoxypropionic Acid)
• 73430-34-9(1,5,9,13,17,21,25,29-Octaoxacyclodotriacontane-2,12,18,28-tetrone)
• 14144-34-4(Propanoic acid,3-ethoxy-, propyl ester)
• 17615-27-9(Ethyl 3-(3-ethoxy-3-oxopropoxy)propanoate)
• 84563-33-7(1,5,9,13-Tetraoxacyclohexadecane-2,12-dione)
• 10606-42-5(Ethyl 3-methoxypropionate)
• 5349-56-4(Propanoic acid,3-methoxy-, propyl ester)
• 14144-40-2(ethyl 3-propoxypropanoate)