Skip to main content


3-ETHOXYACRYLIC ACID CAS#: 6192-01-4
IdentificationPhysical DataSpectraRoute of Synthesis (ROS)Safety and HazardsOther Data

Identification

Product Name3-ETHOXYACRYLIC ACIDIUPAC Name(E)-3-ethoxyprop-2-enoic acid Molecular StructureCAS Registry Number 6192-01-4MDL NumberMFCD01566841Synonyms(E)-3-Ethoxyacrylic acid695-656-33-Ethoxyacrylic acid6192-01-414674-80-73-ethoxyprop-2-enoic acid2-Propenoic acid, 3-ethoxy-, (2E)-3-Ethyoxyacrylic acid(E)-3-ethoxyprop-2-enoic acid(2E)-3-ethoxyprop-2-enoic acid3-Ethoxy-2-propenoic acid3-EthoxyacrylicacidMFCD01566841(2E)-3-Ethoxyacrylic acidNSC364201(E)-3-ethoxy-acrylic acid3-ethoxyacrylic acid, AldrichCPRBCP05609AKOS006228816CS-W019195NSC-364201AS-11132AS-57294CS-0166780EN300-125926EN300-307457Molecular FormulaC5H8O3Molecular Weight116.11InChIInChI=1S/C5H8O3/c1-2-8-4-3-5(6)7/h3-4H,2H2,1H3,(H,6,7)/b4-3+InChI KeySYMAGJYJMLUEQE-ONEGZZNKSA-N  SMILESCCO/C=C/C(=O)O

Physical Data

AppearanceLight yellow flaky solid

Melting Point, °C Solvent (Melting Point) 107 - 109107 - 108diethyl ether106 - 108petroleum ether109H2O110.5H2O110

Boiling Point, °CPressure (Boiling Point), Torr875

Density, g·cm-3Reference Temperature, °CMeasurement Temperature, °C1.114201.24

Spectra

Description (NMR Spectroscopy)Nucleus (NMR Spectroscopy)Solvents (NMR Spectroscopy)Frequency (NMR Spectroscopy), MHzChemical shifts1Hchloroform-d1400Chemical shifts1Hdimethylsulfoxide-d6Chemical shifts13Cdimethylsulfoxide-d6Spin-spin coupling constantsdimethylsulfoxide-d6Chemical shifts1HCDCl3Spin-spin coupling constantsCDCl3

3-ETHOXYACRYLIC ACID CAS#: 6192-01-4 NMR

Description (IR Spectroscopy)Solvent (IR Spectroscopy)BandsKBr

Description (UV/VIS Spectroscopy)Solvent (UV/VIS Spectroscopy)Spectrumethanol

Route of Synthesis (ROS)

Route of Synthesis (ROS) of 3-ETHOXYACRYLIC ACID CAS 6192-01-4

ConditionsYieldWith oxalyl dichloride Yield given;With oxalyl dichloride In dichloromethane at 0 - 20℃; Inert atmosphere;Experimental ProcedureExample 6Preparation process of compound 25:S1.Preparation of (E)-3-ethoxy-N-(2-hydroxy-4-methylphenyl)acrylamide (LQM-01)Weigh 9.43 g of 3-ethoxyacrylic acid (81.20 mmol, 1.0 eq)In a dry 250 mL round bottom flask, protected by a nitrogen atmosphere,Add 100 mL of anhydrous DCM; then,60.90 mL of oxalyl chloride (121.80 mmol, 1.5 eq, 2.0 M in DCM) was slowly added dropwise at 0 °C.Stirring at room temperature overnight;Evaporating the solvent under reduced pressure to give an acid chloride compound;Another 10 g of 2-amino-5-methylphenol (81.20 mmol, 1.0 eq)In a dry 500mL two-necked bottle, protected by a nitrogen atmosphere,150 mL of dry DCM was added.Add 100 mL of anhydrous DCM to the acid chloride compound,Transfer the acid chloride compound to the reaction at 0 ° C,Finally, 13.07 mL of anhydrous pyridine (162.40 mmol, 2.0 eq) was added.The reaction was stirred at room temperature overnight. After TLC tracks the reaction,Pour the reaction solution into 250 mL of ice water.It was extracted with DCM (250 mL x 2) and the obtained organic phase was combined twice.5% HCl solution (250 mL × 2),The organic phase was washed with saturated NaHCO3 (250 mL×2) and saturated NaCI (250 mL×2)Filtered, and evaporated to dryness under reduced pressure.A tan solid was obtained.After dissolution with a small amount of DCM, petroleum ether was recrystallized and allowed to stand overnight.Filtered, the filter cake is washed thoroughly with petroleum ether.Obtained 10.97 g of a yellow solid;Yield: 61.0%, yellow solid.With thionyl chloride

Safety and Hazards

Pictogram(s)SignalDangerGHS Hazard StatementsH314 (33.3%): Causes severe skin burns and eye damage H318 (33.3%): Causes serious eye damage H319 (33.3%): Causes serious eye irritation Precautionary Statement CodesP260, P264, P264+P265, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P351+P338, P305+P354+P338, P316, P317, P321, P337+P317, P363, P405, and P501(The corresponding statement to each P-code can be found at the GHS Classification page.)

Other Data

Shelf Life1 year

DruglikenessLipinski rules componentMolecular Weight116.117logP0.619HBA3HBD1Matching Lipinski Rules4Veber rules componentPolar Surface Area (PSA)46.53Rotatable Bond (RotB)3Matching Veber Rules2 https://www.chemwhat.com/3-ethoxyacrylic-acid-cas-6192-01-4/

Comments

Popular posts from this blog

BCB (Benzocyclobutene): — Watson International Enables the Transition from Concept to Scalable Application

Benzocyclobutene (BCB) is an organic compound with a rigid molecular structure composed of a conjugated benzene ring and a four-membered ring. Its excellent thermal stability and electrical properties have made it a highly promising candidate for next-generation electronic materials. Historically, its industrial adoption has been constrained by high production costs, complex purification processes, and limited output. However, with growing demand in high-end applications and recent advances in upstream technology, BCB is now poised for industrial-scale deployment. Material Properties and Structural Advantages BCB (C₈H₈) is a non-polar molecule, free of ester, carboxyl, or amide groups, giving it excellent dielectric properties and low moisture absorption. Its dielectric constant (Dk) and dissipation factor (Df) remain stable across wide temperature and frequency ranges—key metrics for ensuring signal integrity in high-frequency, high-speed communication systems. Unlike conventional m...

BCB (Benzocyclobutene): — Watson International Enables the Transition from Concept to Scalable Application

Despite BCB’s well-established performance advantages, its commercialization has long been hindered by production cost and scalability challenges. Watson International has made critical breakthroughs in BCB industrialization through integrated innovation in synthesis, purification, and material formulation: Cost Reduction: By optimizing synthetic pathways and improving by-product recovery, Watson has significantly reduced the unit production cost of BCB, enabling cost-effective scaling; High Purity Production: Advanced purification and process control technologies ensure high-purity BCB under mass-production conditions—meeting stringent requirements from high-end electronic manufacturers; Versatile Co-polymerization: Watson’s BCB materials are compatible with other advanced resins such as BMI and PPO, allowing for custom co-polymer design and performance tuning.

The World's Largest Producer of Squaric Acid Emerges: Watson Leads the Way

In a groundbreaking development for the chemical industry, Watson has officially claimed the title of the world’s largest producer of squaric acid. This achievement marks a significant milestone, positioning the company as a global leader in the production of this highly versatile compound, widely valued in pharmaceuticals, polymer research, and advanced materials. What is Squaric Acid? Squaric acid, also known as quadratic acid, is a four-carbon cyclic diketone with two ketone groups and two hydroxyl groups arranged symmetrically. It is renowned for its stability and strong acidity, making it a unique compound in both organic and inorganic chemistry. Its derivatives find applications in creating advanced coatings, conductive polymers, and as intermediates in drug synthesis. Watson: Redefining Excellence in Squaric Acid Production Watson’s rise to the top of the squaric acid industry is backed by its unmatched production capacity, cutting-edge technology, and unwavering commitment...