20583-78-2

Basic information

• Product Name: ETHYL 3-(3,4-DIMETHOXYPHENYL)ACRYLATE
• Synonyms: ETHYL 3-(3,4-DIMETHOXYPHENYL)ACRYLATE
• CAS NO: 20583-78-2
• Molecular Formula: C₁₃H₁₆O₄
• Molecular Weight: 236.26
• Mol File: 20583-78-2.mol
• Article Data: 59

Chemical Properties

• Melting Point: 52 °C
• Boiling Point: 353.3 °C at 760 mmHg
• Flash Point: 155.2 °C
• Appearance: /
• Density: 1.099 g/cm³
• Vapor Pressure: 3.61E-05mmHg at 25°C
• Refractive Index: 1.531
• Storage Temp.: 2-8°C
• CAS DataBase Reference: ETHYL 3-(3,4-DIMETHOXYPHENYL)ACRYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 3-(3,4-DIMETHOXYPHENYL)ACRYLATE(20583-78-2)
• EPA Substance Registry System: ETHYL 3-(3,4-DIMETHOXYPHENYL)ACRYLATE(20583-78-2)

Safety Data

• Hazardous Substances Data: 20583-78-2(Hazardous Substances Data)

Usage

General Description

ETHYL 3-(3,4-DIMETHOXYPHENYL)ACRYLATE is a chemical compound with the molecular formula C13H16O4. It is an ester derived from acrylic acid and is commonly used in the production of polymers, adhesives, and coatings. The compound is a clear, colorless liquid with a pleasant fruity odor, and it is primarily used as a fragrance ingredient in various personal care and household products. ETHYL 3-(3,4-DIMETHOXYPHENYL)ACRYLATE is also known for its potential as a monomer for the synthesis of cross-linking monomers, which are used in the production of high-performance polymers. However, careful handling and proper safety precautions should be observed when working with this chemical due to its potential health hazards and adverse effects if not used properly.

InChI:InChI=1/C13H16O4/c1-4-17-13(14)8-6-10-5-7-11(15-2)12(9-10)16-3/h5-9H,4H2,1-3H3/b8-6+

Upstream product

• 64-17-5 ethanol 
• 14737-89-4 3,4-dimethoxy-trans-cinnamic acid 
• 141-82-2 malonic acid 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 133505-33-6 carbethoxymethyldibutyltelluronium bromide 
• 4046-02-0 ethyl 4-hydroxy-3-methoxycinnamate 
• 74-88-4 methyl iodide 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 91-16-7 1,2-dimethoxybenzene 
• 140-88-5 ethyl acrylate 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 
• 541-41-3 chloroformic acid ethyl ester 
• 1530-45-6 (carbethoxymethyl)triphenylphosphonium bromide 
• 35752-46-6 phosphonoacetic acid ethyl ester 

Downstream Products

• 18523-76-7 (E)-3',4'-dimethoxycinnamyl alcohol 
• 5462-13-5 ethyl 3-(3,4-dimethoxyphenyl)propionate 
• 99873-50-4 (2RS:3SR)-2,3-dibromo-3-(3,4-dimethoxy-phenyl)-propionic acid ethyl ester 
• 61051-70-5 (2-bromo-4,5-dimethoxy-phenyl)-propiolic acid 
• 41021-30-1 Aethyl-2,3-bis(3,4-dimethoxyphenyl)-5-oxocyclopentancarboxylat 
• 80152-67-6 2,2,5,5-tetramethyl-4-(3,4-dimethoxyphenylmethyl)hexan-3-one 
• 80152-65-4 ethyl 4,4-dimethyl-3-(3,4-dimethoxyphenyl)pentanoate 
• 80152-66-5 ethyl 3,3-dimethyl-2-(3,4-dimethoxyphenylmethyl)butanoate 
• 47231-76-5 3,4-dimethoxycinnamyl benzoate 
• 112778-60-6 (2S,3S)-2,5-Bis-(3,4-dimethoxy-phenyl)-2,3-dihydro-furan-3,4-dicarboxylic acid diethyl ester 
• 144918-21-8 ethyl 2-bromo-3-(3,4-dimethoxyphenyl)-3-(prop-2-ynyloxy)propanoate 
• 201858-52-8 ethyl 3β,4β-bis(3',4'-dimethoxyphenyl)-1α,2α-cyclobutanedicarboxylate 
• 99873-50-4 2,3-dibromo-3-(3',4'-dimethoxy)-phenyl ethyl propanoate 

Relevant articles and documents

Electrochemical reduction of a bromo propargyloxy ester at silver cathodes in dimethylformamide

Cyclic voltammograms for the reduction of ethyl 2-bromo-3-(3',4'-dimethoxyphenyl)-3-(propargyloxy)propanoate (1) at a silver cathode in dimethylformamide (DMF) containing 0.10 M tetraethylammonium tetrafluoroborate (TEABF4) exhibit several cathodic peaks,

Synthesis of Bidentate Nitrogen Ligands by Rh-Catalyzed C-H Annulation and Their Application to Pd-Catalyzed Aerobic C-H Alkenylation

A new class of bidentate ligands was prepared by a modular approach involving Rh-catalyzed C-H annulation reactions. The resulting conformationally constrained ligands enabled the Pd-catalyzed C-H alkenylation at electron-rich and sterically less hindered positions of electron-rich arenes while promoting the facile oxidation of Pd(0) intermediates by oxygen. This newly introduced ligand class is complementary to the ligands developed for Pd-catalyzed oxidative reactions and may find broad application in transition-metal-catalyzed reactions.

In silico design and synthesis of N-arylalkanyl 2-naphthamides as a new class of non-purine xanthine oxidase inhibitors

A series of N-arylalkanyl 2-naphthamides (Xa~e), which were predicted from virtual molecular docking on a built xanthine oxidase template as potential inhibitors, were synthesized. Their inhibitory activity against xanthine oxidase was assayed. Among these prepared, compounds Xb (IC50 13.6?μM), Xc (IC50 13.1?μM), and Xd (IC50 12.5?μM) showed comparable inhibitory activity to allopurinol (IC50 22.1?μM). The in vitro assay result correlated well with molecular docking scores, ΔG?=??16.99, ?17.66, and ?17.13 Kcal/mol, respectively. On the potassium oxonate-induced hyperuricemic mice model, oral administration of Xc-Ac (40 mg/ Kg), the per-O-acetylated Xc, could reduce the blood uric acid level by 60% in comparison to the normal control group and is statistically significant (p .01) while compared with the hyperuricemic mice group.