51828-89-8

Basic information

• Product Name: 3-(4-FORMYLPHENYL)-2-PROPENOIC ACID ETHYL ESTER
• Synonyms: 3-(4-FORMYLPHENYL)-2-PROPENOIC ACID ETHYL ESTER;4-FORMYLCINNAMIC ACID ETHYL ESTER;ETHYL 4-FORMYLCINNAMATE
• CAS NO: 51828-89-8
• Molecular Formula: C₁₂H₁₂O₃
• Molecular Weight: 204.22
• Product Categories: Aromatic Cinnamic Acids, Esters and Derivatives
• Mol File: 51828-89-8.mol
• Article Data: 57

Chemical Properties

• Boiling Point: 346.6°Cat760mmHg
• Flash Point: 153.9°C
• Appearance: /
• Density: 1.143g/cm³
• Vapor Pressure: 5.7E-05mmHg at 25°C
• Refractive Index: 1.586
• CAS DataBase Reference: 3-(4-FORMYLPHENYL)-2-PROPENOIC ACID ETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-FORMYLPHENYL)-2-PROPENOIC ACID ETHYL ESTER(51828-89-8)
• EPA Substance Registry System: 3-(4-FORMYLPHENYL)-2-PROPENOIC ACID ETHYL ESTER(51828-89-8)

Safety Data

• Hazardous Substances Data: 51828-89-8(Hazardous Substances Data)

Usage

Description

3-(4-FORMYLPHENYL)-2-PROPENOIC ACID ETHYL ESTER, with the chemical formula C12H12O3, is an ethyl ester derivative of 3-(4-formylphenyl)-2-propenoic acid. It belongs to the class of organic compounds known as cinnamic acids. This chemical compound is characterized by its yellow liquid form and a strong, sweet, floral odor. Its versatile chemical structure makes it suitable for a range of applications across different industries.

Uses

Used in Pharmaceutical Industry:
3-(4-FORMYLPHENYL)-2-PROPENOIC ACID ETHYL ESTER is used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Its unique structure allows it to be a key component in the development of various medications, contributing to the advancement of healthcare and medical treatments.
Used in Food Industry:
As a flavoring agent, 3-(4-FORMYLPHENYL)-2-PROPENOIC ACID ETHYL ESTER enhances the taste profiles of food products. Its strong, sweet, and floral aroma adds depth and complexity to a variety of culinary creations, making it a valuable ingredient in the food and beverage sector.
Used in Cosmetic and Personal Care Industry:
3-(4-FORMYLPHENYL)-2-PROPENOIC ACID ETHYL ESTER is utilized as a fragrance ingredient in cosmetic and personal care products. Its distinctive scent adds a pleasant and appealing fragrance to products such as perfumes, lotions, and creams, enhancing the sensory experience for consumers and contributing to the overall appeal of these products.

InChI:InChI=1/C12H12O3/c1-2-15-12(14)8-7-10-3-5-11(9-13)6-4-10/h3-9H,2H2,1H3/b8-7+

Upstream product

• 64-17-5 ethanol 
• 23359-08-2 4-formylcinnamic acid 
• 104-88-1 4-chlorobenzaldehyde 
• 140-88-5 ethyl acrylate 
• 1122-91-4 4-bromo-benzaldehyde 
• 1791-26-0 4-vinyl-benzaldehyde 
• 623-27-8 terephthalaldehyde, 
• 16173-52-7 4-formylbenzoyl chloride 
• 75-03-6 ethyl iodide 
• 623-73-4 diazoacetic acid ethyl ester 
• 1244044-90-3 ethyl (2E)-3-{[(cyclohexylamino)carbonyl]}phenylacrylate 
• 15164-44-0 p-(iodophenyl)carboxaldehyde 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 

Downstream Products

• 104478-10-6 ethyl 4-[2-all-trans-(2'-naphthyl)-propenyl]-cinnamate 
• 107859-98-3 ethyl 3-[4-(hydroxymethyl)phenyl]propanoate 
• 1604814-12-1 (E)-3-(4-formylphenyl)allyl methyl carbonate 
• 1604814-19-8 methyl (2Z,4E)-2-((dimethyl(phenyl)silyl)(phenyl)methylene)-5-(4-formylphenyl)pent-4-enoate 
• 530145-11-0 (E)-ethyl 3-(4-(hydroxymethyl)phenyl)prop-2-enoate 
• 445483-72-7 3-(4-formyl-phenyl)-propionic acid ethyl ester 
• 1448685-38-8 C₁₉H₂₇NO₄ 
• 1448685-40-2 C₂₀H₂₇NO₆ 
• 1448685-41-3 C₂₇H₃₄N₄O₇ 
• 1448685-42-4 C₂₇H₃₂N₄O₆ 
• 1448685-43-5 C₂₇H₃₄N₄O₄ 
• 1448685-44-6 C₃₁H₄₂N₄O₆ 
• 1448685-45-7 C₃₁H₄₀Cl₂N₄O₄ 

Relevant articles and documents

Photoinduced Regioselective Olefination of Arenes at Proximal and Distal Sites

The Fujiwara-Moritani reaction has had a profound contribution in the emergence of contemporary C-H activation protocols. Despite the applicability of the traditional approach in different fields, the associated reactivity and regioselectivity issues had

Pd/Cu-Free Cobalt-Catalyzed Suzuki and Heck Using Green Bio-Magnetic Hybrid and DFT-Based Theoretical Study

Abstract: Several highly efficient and magnetically recyclable cobalt catalytic systems were prepared using magnetic chitosan and some safe and available organic compounds (Co-ligand@MNPs/Ch). The structure of these nanocomposites was confirmed by various physicochemical techniques such as FT-IR, XRD, TGA, VSM, TEM, SEM, CHNS and ICP-OES. These nano composites exhibit remarkable catalytic efficiency for Suzuki and Heck cross-coupling reactions in mild and green reaction conditions. The facile accessibility of starting materials, possible performance in air and eco-friendly conditions are merits of our catalysts. In addition, to describe and go insight to role and effect of ligands present in these catalysts, electrostatic interactions, density functional theory (DFT) model in molecular method were employed. Graphic Abstract: [Figure not available: see fulltext.]

Sulphonic acid functionalized porphyrin anchored with a: Meso -substituted triazolium ionic liquid moiety: A heterogeneous photo-catalyst for metal/base free C-C cross-coupling and C-N/C-H activation using aryl chloride under visible light irradiation

We report an easy process to synthesize sulphonic acid functionalized porphyrin, anchored with a meso-substituted triazolium ionic liquid moiety (SAFPTILM) for metal/base free C-C cross-coupling and C-N/C-H activation using aryl chloride under visible light irradiation. The acid strength has been measured based on the Hammett indicator. The SAFPTILM photocatalyst comprising 18 π-conjugated electronic systems with the chromophore substituents in the meso-position can provide rapid electronic conducting channels during photocatalysis under the irradiation of visible light. It was found that SAFPTILM is an efficient photocatalyst for the Heck, Sonogashira, Buchwald, Ullmann/Fittig coupling and C-H activation of phenols with different aryl chlorides in the absence of a base/noble metal, using 5 W LED (yellow) light under ambient conditions. The photocatalyst with low band gap (1.55 eV) comprising conjugation, favors coupling reaction of unactivated aryl chlorides, by easy excitation of electrons and transfer to the conjugated benzimidazolium based phenylenediamine support delaying the recombination of photoinduced electron-hole pairs.