Cai, Zhenping et al. published their research in Green Chemistry in 2021 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Product Details of 763-69-9

One-pot production of diethyl maleate via catalytic conversion of raw lignocellulosic biomass was written by Cai, Zhenping;Chen, Rujia;Zhang, Hao;Li, Fukun;Long, Jinxing;Jiang, Lilong;Li, Xuehui. And the article was included in Green Chemistry in 2021.Product Details of 763-69-9 The following contents are mentioned in the article:

The conversion of lignocellulose into a value-added chem. with high selectivity is of great significance but is a big challenge due to the structural diversities of biomass components. Here, we have reported an efficient approach for the one-step conversion of raw lignocellulose into di-Et maleate by the polyoxometalate ionic liquid [BSmim]CuPW12O40 in ethanol under mild conditions. The results reveal that all of the fractions in biomass, i.e., cellulose, lignin and hemicellulose, were simultaneously converted into di-Et maleate (DEM), achieving a 329.6 mg g-1 yield and 70.3% selectivity from corn stalk. Importantly, the performance of the ionic liquid catalyst [BSmim]CuPW12O40 was nearly twice that of CuPW12O40, which can be attributed to the lower incorporation of the Cu2+ site in [BSmim]CuPW12O40. Hence, this process opens a promising route for producing bio-based bulk chems. from raw lignocellulose without any pretreatment. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Product Details of 763-69-9).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Product Details of 763-69-9

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Ledauphin, Jerome et al. published their research in Journal of Agricultural and Food Chemistry in 2004 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Synthetic Route of C7H14O3

Identification of Trace Volatile Compounds in Freshly Distilled Calvados and Cognac Using Preparative Separations Coupled with Gas Chromatography-Mass Spectrometry was written by Ledauphin, Jerome;Saint-Clair, Jean-Francois;Lablanquie, Odile;Guichard, Hugues;Founier, Nicole;Guichard, Elisabeth;Barillier, Daniel. And the article was included in Journal of Agricultural and Food Chemistry in 2004.Synthetic Route of C7H14O3 The following contents are mentioned in the article:

GC-MS using both electron impact and chem. ionization detection modes led to the determination of the volatile composition of 2 samples of freshly distilled Cognac and 2 samples of freshly distilled Calvados. A total of 169 volatile compounds were directly identified in dichloromethane extracts obtained by liquid-liquid extraction Trace compounds present in both spirits were characterized with the help of preparative separations In a 1st step, groups of compounds were separated by preparative GC, and the fractions were analyzed on a polar stationary phase by GC-MS. In a 2nd step, silica gel fractionation was used to sep. them by polarity. In 331 compounds, of which 162 can be considered as trace compounds, were characterized in both freshly distilled Cognac and Calvados. Of these, 39 are common to both spirits; 30 are specific to Cognac with numerous hexenyl esters and norisoprenoidic derivatives, whereas 93 are specific to Calvados with compounds such as unsaturated alcs., phenolic derivatives, and unsaturated aldehydes. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Synthetic Route of C7H14O3).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Synthetic Route of C7H14O3

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Rios-Reina, Rocio et al. published their research in Food Research International in 2018 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Application In Synthesis of Ethyl 3-ethoxypropanoate

Sampling methods for the study of volatile profile of PDO wine vinegars. A comparison using multivariate data analysis was written by Rios-Reina, Rocio;Morales, M. Lourdes;Garcia-Gonzalez, Diego L.;Amigo, Jose M.;Callejon, Raquel M.. And the article was included in Food Research International in 2018.Application In Synthesis of Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

High-quality wine vinegars have been registered in Spain under protected designation of origin (PDO): “Vinagre de Jerez”, “Vinagre de Condado de Huelva” and “Vinagre de Montilla-Moriles”. The raw material, production and aging processes determine their quality and their aromatic composition Vinegar volatile profile is usually analyzed by gas chromatog.-mass spectrometry (GC-MS), being necessary a previous extraction step. Thus, three different sampling methods (Headspace solid phase microextraction “HS-SPME”, Headspace stir bar sorptive extraction “HSSE” and Dynamic headspace extraction “DHS”) were studied for the anal. of the volatile composition of Spanish PDO wine vinegars. Multivariate curve resolution (MCR) was used to solve chromatog. problems, improving the results obtained. Principal component anal. (PCA) showed that not all the sampling methods were equally suitable for the characterization and differentiation between PDOs and categories, being HSSE the technique that made able the best vinegar characterization. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Application In Synthesis of Ethyl 3-ethoxypropanoate).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Application In Synthesis of Ethyl 3-ethoxypropanoate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Kuo, Y. D. et al. published their research in Experimental Thermal and Fluid Science in 2016 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Product Details of 763-69-9

Experimental study of surface heating by a high speed exhaust plume was written by Kuo, Y. D.;Smith, N. S. A.;Honnery, D. R.. And the article was included in Experimental Thermal and Fluid Science in 2016.Product Details of 763-69-9 The following contents are mentioned in the article:

Airframe surface heating by gas turbine plume is an ongoing issue in aerospace applications. This paper presents the practicability of a smaller scale system based on a micro gas turbine which offers verisimilitude and realism to the actual airframe surface heating by a full scale engine exhaust plume flow. A thin flat plate made from 7075-T6 aluminum alloy was placed at X = 7D downstream of the nozzle exit of the gas turbine. Nozzle exit flow temperature ranged from 850 K to 920 K and Reynolds number over the sample plate ranged from 3.8 × 104 to 2.6 × 105. The average Nusselt number was found to be correlated to CRemPrn with m = 0.42, n = 0.33, C = 0.094 for parallel plume flow over the sample plate at X = 7D and Z = 0D. It was also found that coefficient C can be scaled by velocity magnitude ratio with respect to the plume center if the sample was positioned away from the center of the jet plume. Heat transfer by IR radiation was found to be less than 2% compared to the overall heat flux. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Product Details of 763-69-9).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Product Details of 763-69-9

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Pereira, Vanda et al. published their research in Food Chemistry in 2014 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: Ethyl 3-ethoxypropanoate

Volatile profile of Madeira wines submitted to traditional accelerated ageing was written by Pereira, Vanda;Cacho, Juan;Marques, Jose C.. And the article was included in Food Chemistry in 2014.Recommanded Product: Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

The evolution of monovarietal fortified Madeira wines forced-aged by traditional thermal processing (estufagem) were studied in terms of volatiles. SPE extracts were analyzed by GC-MS before and after heating at 45°C for 3 mo (standard) and at 70°C for 1 mo (overheating). One hundred and ninety volatile compounds were identified, 53 of which were only encountered in baked wines. Most chem. families increased after standard heating, especially furans and esters, up to 61 and 3-fold, resp. On the contrary, alcs., acetates and fatty acids decreased after heating. Varietal aromas, such as Malvasia’s monoterpenic alcs. were not detected after baking. The accelerated aging favored the development of some volatiles previously reported as typical aromas of finest Madeira wines, particularly phenylacetaldeyde, β-damascenone and 5-ethoxymethylfurfural. Addnl., Et butyrate, Et 2-methylbutyrate, Et caproate, Et isovalerate, guaiacol, 5-hydroxymethylfurfural and γ-decalactone were also found as potential contributors to the global aroma of baked wines. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Recommanded Product: Ethyl 3-ethoxypropanoate).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: Ethyl 3-ethoxypropanoate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Zhao, Yuping et al. published their research in Sepu in 2008 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Quality Control of Ethyl 3-ethoxypropanoate

Extraction, preparation and identification of volatile compounds in Changyu XO brandy was written by Zhao, Yuping;Li, Jiming;Xu, Yan;Duan, Hui;Fan, Wenlai;Zhao, Guang’ao. And the article was included in Sepu in 2008.Quality Control of Ethyl 3-ethoxypropanoate The following contents are mentioned in the article:

A method for the preparation of volatile compounds in Changyu XO brandy was established. The volatile compounds were extracted using liquid-liquid extraction and then were separated into two fractions, namely, the acidic/water-soluble fraction and the neutral/basic fraction. The neutral/basic fraction was furthermore separated into 4 fractions using silica gel normal phase chromatog., and each fraction was then concentrated and analyzed using gas chromatog.-mass spectrometry (GC-MS). In comparison with the pure standards and the retention indexes (RIs) reported in the literature, a total of 302 volatile compounds were identified in Changyu XO brandy, including 30 alcs., 35 aldehydes and ketones, 20 carboxylic acids, 104 esters, 24 substituted benzenes and derivatives, 14 phenolic derivatives, 14 acetals, 16 furan derivatives, 22 terpenic and norisoprenoidic derivatives and 23 others. It was demonstrated that this method of preparation was effective for the separation and concentration of volatile compounds in Changyu XO brandy. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Quality Control of Ethyl 3-ethoxypropanoate).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Quality Control of Ethyl 3-ethoxypropanoate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Mulero, A. et al. published their research in Journal of Physical and Chemical Reference Data in 2022 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Electric Literature of C7H14O3

Recommended Correlations for the Surface Tension of Aromatic, Polyfunctional, and Glyceride Esters was written by Mulero, A.;Cachadina, I.;Vegas, A.. And the article was included in Journal of Physical and Chemical Reference Data in 2022.Electric Literature of C7H14O3 The following contents are mentioned in the article:

Surface tension values for 79 esters, including aromatics, polyfunctional, and glycerides, have been compiled from databases, books, and papers in the literature. The data have been carefully screened, and finally, 1517 values were selected. Each fluid dataset has been fitted with the Guggenheim-Katayama correlation with two or four adjustable parameters. Recommended correlations are proposed for each ester, providing mean absolute deviations below 0.50 mN/m for 77 of them, mean absolute percentage deviations below 1.7% for 76 of them, and percentage deviations below 10%, except for four data out of the 59 selected for tricaprylin. The highest deviations found are due to the disagreement between the data obtained from different sources and not to an inadequate math. form of the correlation model. These correlations are added to the collection of those previously proposed for different fluids, including common substances, alcs., refrigerants, organic acids, n-alkanes, and 80 other esters. (c) 2022 American Institute of Physics. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Electric Literature of C7H14O3).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Electric Literature of C7H14O3

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Teodorescu, F. et al. published their research in Catalysis Letters in 2014 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Category: esters-buliding-blocks

Addition of Alcohols to Acrylic Compounds Catalyzed by Mg-Al LDH was written by Teodorescu, F.;Deaconu, M.;Bartha, E.;Zavoianu, R.;Pavel, O. D.. And the article was included in Catalysis Letters in 2014.Category: esters-buliding-blocks The following contents are mentioned in the article:

This study reports the preparation of hydrotalcite with Mg/Al molar ratio 3 by co-precipitation under low suprasatn. conditions of Mg and Al nitrated solutions with Na2CO3 and NaOH at pH 10. The solid was thermally decomposed at 460° in air atm. in order to obtain mixed oxides which, by means of memory effect, can reconstruct the hydrotalcite structure by hydration with bi-distilled water. The hydrotalcite and reconstructed samples by memory effect were characterized by elemental anal., powder x-ray diffraction, DRIFT and TG-DTG. Determination of the catalysts surface base sites was made using a method based on the irreversible adsorption of organic acids with different pKa values and N2 adsorption-desorption isotherms. The catalytic activity of these solids was evaluated in 1,4-addition of saturated linear alcs. to different acrylic compounds All these reactions arose with high selectivity in the desired product. No byproducts were detected by means of GC-MS chromatog. and 1H NMR. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Category: esters-buliding-blocks).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Category: esters-buliding-blocks

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Wang, Chih-Feng et al. published their research in Polymers (Basel, Switzerland) in 2020 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Reference of 763-69-9

Tuning the wettability and surface free energy of poly(vinylphenol) thin films by modulating hydrogen-bonding interactions was written by Wang, Chih-Feng;Ejeta, Dula Daksa;Wu, Jian-Yi;Kuo, Shiao-Wei;Lin, Ching-Hsuan;Lai, Juin-Yih. And the article was included in Polymers (Basel, Switzerland) in 2020.Reference of 763-69-9 The following contents are mentioned in the article:

The ability to tune the surface properties of a polymer film in a simple and effective manner is important for diverse biol., industrial, and environmental applications. In this work, we investigated whether or not the surface free energy of poly(vinyl phenol; PVPh) can be tuned by adjusting the casting solvent and the thermal treatment time, which alters the proportions of intraand intermol. hydrogen bonding interactions. Compared to the untreated sample, in THF system, the thermal treatment resulted in a lower proportion of intermol. hydrogen bonds and a concomitant decrease in the surface free energy (from 39.3 to 18.8 mJ/m2). In contrast, the thermal treatment in propylene glycol Me ether acetate (PGMEA) and ethyl-3-ethoxypropionate (EEP) systems increased the proportion of intermol. hydrogen bonds and the surface free energy of the polymer thin films, from 45.0 to 54.3 mJ/m2 for PGMEA and from 45.5 to 52.9 mJ/m2 for EEP. Controlling intermol. hydrogen-bonding interactions is a unique and easy method for tuning the surface free energies of polymer substances. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Reference of 763-69-9).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Reference of 763-69-9

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Galhenage, Teluka Pasan et al. published their research in Biofouling in 2022 | CAS: 763-69-9

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Synthetic Route of C7H14O3

Durable siloxane-polyurethane coatings for mitigating freshwater mussel fouling was written by Galhenage, Teluka Pasan;Stafslien, Shane J.;Skaja, Allen;Webster, Dean C.. And the article was included in Biofouling in 2022.Synthetic Route of C7H14O3 The following contents are mentioned in the article:

Siloxane-polyurethane hybrid coatings were assessed for biofouling control caused by freshwater mussels. Invasive species such as zebra (Dreissena polymorpha) and quagga (Dreissena bugensis) mussels have rapidly spread through the waterways in the United States causing major concerns in reservoir infrastructure and freshwater lakes. Current coating solutions such as biocidal anti-fouling coatings are not suitable given the released biocides which may accumulate in reservoirs. Biocide free fouling release coatings based on silicone elastomers do not have adequate mech. durability. The siloxane-polyurethane (SiPU) coatings were evaluated using model organism laboratory assays and real-life performance was evaluated in the freshwater field environment. Two coating compositions displayed excellent performance in field trials for up to 2+ years. The surface anal. experiments of the coatings indicate that the morphol. of the coatings is affected by the formulations’ solvent choice. These coatings show great promise in mitigating biofouling predominated by freshwater mussels. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Synthetic Route of C7H14O3).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Synthetic Route of C7H14O3

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics