199679-44-2

Basic information

• Product Name: 3-[4-(2-HYDROXY-ETHOXY)-PHENYL]-ACRYLIC ACID
• Synonyms: RARECHEM AL BK 0433;3-[4-(2-HYDROXY-ETHOXY)-PHENYL]-ACRYLIC ACID
• CAS NO: 199679-44-2
• Molecular Formula: C11H12O4
• Molecular Weight: 208.21
• Product Categories: pharmacetical
• Mol File: 199679-44-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-[4-(2-HYDROXY-ETHOXY)-PHENYL]-ACRYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[4-(2-HYDROXY-ETHOXY)-PHENYL]-ACRYLIC ACID(199679-44-2)
• EPA Substance Registry System: 3-[4-(2-HYDROXY-ETHOXY)-PHENYL]-ACRYLIC ACID(199679-44-2)

Safety Data

• Hazardous Substances Data: 199679-44-2(Hazardous Substances Data)

Usage

General Description

3-[4-(2-hydroxy-ethoxy)-phenyl]-acrylic acid is a chemical compound with the molecular formula C11H12O4. It is a derivative of acrylic acid and contains a phenyl group with an attached ethoxy and hydroxy group. 3-[4-(2-HYDROXY-ETHOXY)-PHENYL]-ACRYLIC ACID is commonly used in the production of pharmaceuticals and as a building block for the synthesis of various organic compounds. It has potential applications in the area of drug discovery and development, as well as in the field of materials science. The presence of the hydroxy and ethoxy groups in the phenyl ring makes this compound particularly useful in organic synthesis and medicinal chemistry. Overall, 3-[4-(2-hydroxy-ethoxy)-phenyl]-acrylic acid is an important chemical building block with diverse applications in various industries.

Upstream product

• 7400-08-0 para-coumaric acid 
• 107-07-3 2-chloro-ethanol 
• 141-82-2 malonic acid 
• 22042-73-5 4-(2-hydroxy-ethoxy)-benzaldehyde 
• 7400-08-0 p-Coumaric Acid 
• 540-51-2 2-bromoethanol 

Downstream Products

• 1609030-91-2 (E)-3-(4-(2-hydroxyethoxy)phenyl)-N-(2-(2-methyl-1H-indol-1-yl)ethyl)acrylamide 
• 106737-07-9 3-[4-(2-chloro-ethoxy)-phenyl]-propionic acid-(2-dimethylamino-ethyl ester) 
• 100126-93-0 3-[4-(2-chloro-ethoxy)-phenyl]-propionic acid 
• 51822-73-2 4-(2-hydroxyethoxy)phenylpropanoic acid 

Relevant articles and documents

Polyethylene ferulate (PEF) and congeners: polystyrene mimics derived from biorenewable aromatics

Ferulic acid and p-coumaric acid are abundant, biorenewable precursors for the synthesis of polyethylene ferulate (PEF) and polyethylene coumarate (PEC), as well as cognate copolymers with prescribed hydrogenation of the main-chain double bond. By controlling the comonomer feed ratios, copolymers with tunable thermal properties are obtained, including the thermal range occupied by polystyrene (PS).

Purification, structural characterization, and modification of organosolv wheat straw lignin

Biolignin, a wheat straw lignin produced by acetic acid/formic acid/water hydrolysis, was characterized by 31P and 13C-1H 2D NMR spectroscopy and by size-exclusion chromatography. Biolignin is a mixture of low molar mass compounds (Mn = 1660 g/mol) made up of S, G, and H units and of coumaric and ferulic acid units. β-5 and β-O-4 interunit linkages are partially acylated in the γ-position by acetate and p-coumarate groups. Deacylated samples with a low content of contaminants were obtained by combining alkaline hydrolysis and solvent extraction. The high phenolic OH content found by 31P NMR reflects the presence of condensed aromatic units, such as 5-5 units. Reaction of purified lignin with ethanol and ethane-1,2-diol yielded esterified lignins much more soluble than Biolignin in common organic solvents. During this reaction, the secondary OH of β-O-4 linkages was simultaneously etherified. Phenol hydroxyethylation by 2-chloroethanol yielded samples containing only aliphatic hydroxyl groups.