20349-89-7

Basic information

• Product Name: METHYL 3-(2-HYDROXYPHENYL)PROPIONATE
• Synonyms: METHYL 3-(2-HYDROXYPHENYL)PROPANOATE;METHYL 3-(2-HYDROXYPHENYL)PROPIONATE;3-(2-Hydroxyphenyl)propionicacidmethylester;methyl 2'-hydroxyhydrocinnamate;Methyl 3-(2-hydroxyphenyl)propanoate, 95%+;3-(2-Hydroxyphenyl)propionate;Methyl 3-(2-hydroxyphenyl)
• CAS NO: 20349-89-7
• Molecular Formula: C₁₀H₁₂O₃
• Molecular Weight: 180.2
• Mol File: 20349-89-7.mol
• Article Data: 20

Chemical Properties

• Melting Point: 40-42°C
• Boiling Point: 280.2°C at 760 mmHg
• Flash Point: 116.6°C
• Appearance: /
• Density: 1.146g/cm³
• Vapor Pressure: 0.00225mmHg at 25°C
• Refractive Index: 1.532
• PKA: 10.02±0.30(Predicted)
• CAS DataBase Reference: METHYL 3-(2-HYDROXYPHENYL)PROPIONATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 3-(2-HYDROXYPHENYL)PROPIONATE(20349-89-7)
• EPA Substance Registry System: METHYL 3-(2-HYDROXYPHENYL)PROPIONATE(20349-89-7)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Safety Statements: 24/25
• Hazardous Substances Data: 20349-89-7(Hazardous Substances Data)

Usage

General Description

Methyl 3-(2-hydroxyphenyl)propionate is an organic compound consisting of a methyl ester of 3-(2-hydroxyphenyl)propionic acid. It is commonly used in the fragrance and flavor industry due to its pleasant, sweet, and slightly floral odor. This chemical is often used in the formulation of perfumes, soaps, and other scented household products. It is also used as a flavoring agent in food products and beverages. Additionally, it has been studied for its potential medicinal properties, including anti-inflammatory and antioxidant effects. Overall, methyl 3-(2-hydroxyphenyl)propionate is a versatile compound with various applications in the industry and potential health benefits.

InChI:InChI=1/C10H12O3/c1-13-10(12)7-6-8-4-2-3-5-9(8)11/h2-5,11H,6-7H2,1H3

Upstream product

• 67-56-1 methanol 
• 119-84-6 C₆H₄(CH₂CH₂C(O)O) 
• 83-33-0 inden-1-one 
• 77086-38-5 ketene t-butyldimethylsilyl methyl acetal 
• 538342-16-4 3-methoxycarbonyl-4H-1,2-benzoxazine 
• 6236-69-7 methyl 2-hydroxycinnamate 
• 91-64-5 coumarin 
• 495-78-3 3-(2-hydroxyphenyl)propionic acid 
• 74-88-4 methyl iodide 
• 103-25-3 3-phenylpropanoic acid methyl ester 
• 90-02-8 salicylaldehyde 
• 100-52-7 benzaldehyde 
• 42251-12-7 α-nitro cinnamate de methyle E 
• 40149-56-2 Methyl α-nitro-β-phenylpropionate 

Downstream Products

• 83281-55-4 3-(2-Oxiranylmethoxy-phenyl)-propionic acid methyl ester 
• 327189-16-2 methyl 3-[2-[3-[4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolyl]propoxy]phenyl]propionate 
• 936329-18-9 methyl 3-(2-(3-chloropropoxy)phenyl)propanoate 
• 936328-06-2 methyl 3-(2-{[(2S)-2-methyloxiran-2-yl]methoxy}phenyl)propanoate 
• 1228808-22-7 methyl 3-(2-(dichlorophosphoryloxy)phenyl)propanoate 
• 220285-28-9 3-(2-ethoxyphenyl)propionic acid 
• 67-56-1 methanol 

Relevant articles and documents

Microbial reduction of coumarin, psoralen, and xanthyletin by Glomerella cingulata

Microbial transformation of coumarin, psoralen, and xanthyletin was performed with the fungus Glomerella cingulata. The main reaction pathways involved reduction at α,β-unsaturated δ-lactone ring on coumarin analogue. Coumarin was metabolized by G. cingul

LYSOPHOSPHATIDYLSERINE DERIVATIVE

PROBLEM TO BE SOLVED: To provide a lysophosphatidylserine derivative or salt thereof. SOLUTION: The present invention provides a lysophosphatidylserine derivative or salt thereof, or a pharmaceutical composition or lysophosphatidylserine receptor function modulator including the compound or salt thereof. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

Hydrogenation of coumarin to octahydrocoumarin over a Ru/C catalyst

The production of octahydrocoumarin, which can serve as a replacement for toxic coumarin, was investigated using 5% Ru on active carbon (Ru/C) as the catalyst for the hydrogenation of coumarin. The hydrogenation was studied by optimizing the reaction conditions (pressure, solvent and coumarin concentration). The activity and selectivity of the Ru/C catalyst were compared for different solvents. The mechanism of coumarin hydrogenation was deduced. The formation of side products was explained. The optimal hydrogenation reaction conditions were: 130 °C, 10 MPa, 60 wt% coumarin in methanol, and 0.5 wt% (based on coumarin) of Ru/C catalyst. At the complete conversion of coumarin, the selectivity to the desired product was 90%.