34708-60-6

Basic information

• Product Name: 3-(3-HYDROXY-PHENYL)-PROPIONIC ACID ETHYL ESTER
• Synonyms: Benzenepropanoic acid, 3-hydroxy-, ethyl ester;3-(3-HYDROXY-PHENYL)-PROPIONIC ACID ETHYL ESTER;Ethyl 3-(m-hydroxyphenyl)propionate;Ethyl 3-(3-hydroxyphenyl)propanoate
• CAS NO: 34708-60-6
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 194.23
• Mol File: 34708-60-6.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 309.699°C at 760 mmHg
• Flash Point: 129.476°C
• Appearance: /
• Density: 1.118g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.527
• PKA: 9.94±0.10(Predicted)
• CAS DataBase Reference: 3-(3-HYDROXY-PHENYL)-PROPIONIC ACID ETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3-HYDROXY-PHENYL)-PROPIONIC ACID ETHYL ESTER(34708-60-6)
• EPA Substance Registry System: 3-(3-HYDROXY-PHENYL)-PROPIONIC ACID ETHYL ESTER(34708-60-6)

Safety Data

• Hazardous Substances Data: 34708-60-6(Hazardous Substances Data)

Usage

General Description

3-(3-Hydroxy-phenyl)-propionic acid ethyl ester is a chemical compound with the molecular formula C11H14O3. It is a derivative of 3-hydroxyphenyl propionic acid and is commonly used in the pharmaceutical and fragrance industries. 3-(3-HYDROXY-PHENYL)-PROPIONIC ACID ETHYL ESTER has potential applications in the synthesis of various pharmaceutical drugs and as a scent ingredient in perfumes and personal care products. It is also known for its anti-inflammatory properties, making it an important compound in the development of drugs for the treatment of inflammatory conditions. 3-(3-Hydroxy-phenyl)-propionic acid ethyl ester is a versatile chemical with a wide range of potential uses and applications in various industries.

InChI:InChI=1/C11H14O3/c1-2-14-11(13)7-6-9-4-3-5-10(12)8-9/h3-5,8,12H,2,6-7H2,1H3

Upstream product

• 140-88-5 ethyl acrylate 
• 591-20-8 3-Bromophenol 
• 4046-02-0 ethyl 4-hydroxy-3-methoxycinnamate 
• 14755-02-3 3-hydroxycinnamic acid 
• 64-17-5 ethanol 
• 621-54-5 3-(3-hydroxyphenyl)-propanoic acid 
• 96251-92-2 (E)-3-(3-hydroxyphenyl)acrylic acid ethyl ester 
• 3943-96-2 3-(3-hydroxyphenyl)acrylic acid ethyl ester 
• 14755-02-3 3-hydroxy-trans-cinnamic acid 

Downstream Products

• 75849-10-4 ethyl 3-<3-(benzyloxy)phenyl>propanoate 
• 156005-68-4 3-{3-[3-(4-Acetyl-phenoxy)-propoxy]-phenyl}-propionic acid ethyl ester 
• 156005-47-9 3-<3-(allyloxy)phenyl>propionic acid ethyl ester 
• 156005-38-8 3-[3-(3-Bromo-propoxy)-phenyl]-propionic acid ethyl ester 
• 174813-74-2 ethyl 3-(3-butoxyphenyl)propanoate 
• 116609-01-9 3-(3-ethoxy-phenyl)-propionic acid ethyl ester 
• 1027377-50-9 3-(3-Isobutoxy-phenyl)-propionic acid ethyl ester 
• 156175-93-8 3-[3-(3-Fluoro-propoxy)-phenyl]-propionic acid ethyl ester 
• 1027051-93-9 3-[3-(4,4,4-Trifluoro-butoxy)-phenyl]-propionic acid ethyl ester 
• 156175-97-2 3-(3-sec-Butoxy-phenyl)-propionic acid ethyl ester 
• 156175-82-5 ethyl 3-(3-propoxyphenyl)propanoate 
• 494865-03-1 3-{3-[3,3-bis-(4-bromo-phenyl)-allyloxy]-phenyl}-propionic acid ethyl ester 
• 351490-88-5 ethyl 4-formyl-3-hydroxybenzenepropionate 
• 882069-35-4 3-[3-(3-{3-[2,2,2-trifluoro-1-(4-methoxy-benzyloxy)-1-trifluoromethyl-ethyl]-phenoxy}-propoxy)-phenyl]-propionic acid ethyl ester 

Relevant articles and documents

Preparation method of aza compounds

The invention discloses a preparation method of aza compounds N-((5-(3-hydroxyphenyl)-2H-1,2,4-triazole-3-ol)methyl)-N-propyl-1-amine. 3-(3-hydroxyphenyl)ethyl acrylate serves as an initial material, a target product 7 is obtained through reduction, acyla

COMPOSITIONS FOR THE TREATMENT OF KIDNEY AND/OR LIVER DISEASE

The present invention relates to novel compounds and their use in the prophylactic and/or therapeutic treatment of kidney and/or liver disease.

Chemo- and Regioselective Hydrogenolysis of Diaryl Ether C-O Bonds by a Robust Heterogeneous Ni/C Catalyst: Applications to the Cleavage of Complex Lignin-Related Fragments

We report the chemo- and regioselective hydrogenolysis of the C-O bonds in di-ortho-substituted diaryl ethers under the catalysis of a supported nickel catalyst. The catalyst comprises heterogeneous nickel particles supported on activated carbon and furnishes arenes and phenols in high yields without hydrogenation. The high thermal stability of the embedded metal particles allows C-O bond cleavage to occur in highly substituted diaryl ether units akin to those in lignin. Preliminary mechanistic experiments show that this catalyst undergoes sintering less readily than previously reported catalyst particles that form from a solution of [Ni(cod)2].