4112-89-4

Basic information

• Product Name: FEMA 2535
• Synonyms: Benzeneaceticacid,2-methoxyphenylester;FEMA 2535;GUAIACOL PHENYL ACETATE;GUAIACYL PHENYLACETATE;2-methoxyphenyl phenylacetate;GUAIACYL PHENYLACETATE 98+%;GUAIACYL PHENYL ACETATE 98%;Benzeneacetic acid, 2-methoxyphenyl
• CAS NO: 4112-89-4
• Molecular Formula: C₁₅H₁₄O₃
• Molecular Weight: 242.27
• EINECS: 223-898-8
• Product Categories: Alphabetical Listings;Flavors and Fragrances;G-H
• Mol File: 4112-89-4.mol

Chemical Properties

• Melting Point: 40-43 °C(lit.)
• Boiling Point: 354.2 °C at 760 mmHg
• Flash Point: >230 °F
• Appearance: /
• Density: 1.144
• Vapor Pressure: 3.39E-05mmHg at 25°C
• Refractive Index: 1.562
• Merck: 13,4568
• CAS DataBase Reference: FEMA 2535(CAS DataBase Reference)
• NIST Chemistry Reference: FEMA 2535(4112-89-4)
• EPA Substance Registry System: FEMA 2535(4112-89-4)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 4112-89-4(Hazardous Substances Data)

Usage

Uses

Used in Flavor and Fragrance Industry:
FEMA 2535 is used as a flavoring agent for its woody, spicy, and smoky flavor. It is commonly used in the flavor and fragrance industry to add depth and complexity to various products, such as perfumes, colognes, and scented candles.
Used in Food and Beverage Industry:
FEMA 2535 is used as a flavoring agent in the food and beverage industry to enhance the taste and aroma of various products, such as baked goods, confections, and alcoholic and non-alcoholic beverages. Its sweet, phenolic, spicy, anisic taste characteristics make it a versatile ingredient for creating unique flavor profiles.
Used in Pharmaceutical Industry:
FEMA 2535 may also have potential applications in the pharmaceutical industry, particularly in the development of drugs that target specific receptors or pathways. Its chemical properties and interactions with biopolymers and macromolecules make it a promising candidate for further research and development in this field.

InChI:InChI=1/C15H14O3/c1-17-13-9-5-6-10-14(13)18-15(16)11-12-7-3-2-4-8-12/h2-10H,11H2,1H3

Upstream product

• 90-05-1 2-methoxy-phenol 
• 103-80-0 phenylacetyl chloride 
• 103-82-2 phenylacetic acid 

Downstream Products

• 58451-99-3 3'-Hydroxy-4'-methoxy-2-phenylacetophenon 
• 73049-08-8 4-(1-Hydroxy-2-phenyl-ethyl)-2-methoxy-phenol 
• 3391-75-1 2-methoxy-4-((E)-phenylethenyl)phenol 
• 66476-02-6 1-(4-hydroxy-3-methoxyphenyl)-2-phenylethan-1-one 
• 66475-99-8 2-Phenylacetoxy-4-phenylacetylanisol 

Relevant articles and documents

Evaluating aryl esters as bench-stable C(1)-ammonium enolate precursors in catalytic, enantioselective Michael addition-lactonisations

An evaluation of a range of aryl, alkyl and vinyl esters as prospective C(1)-ammonium enolate precursors in enantioselective Michael addition-lactonisation processes with (E)-trifluoromethylenones using isothiourea catalysis is reported. Electron deficient aryl esters are required for reactivity, with 2,4,6-trichlorophenyl esters providing optimal product yields. Catalyst screening showed that tetramisole was the most effective isothiourea catalyst, giving the desired dihydropyranone product in excellent yield and stereoselectivity (up to 90 : 10 dr and 98 : 2 er). The scope and limitations of this process have been evaluated, with a range of diester products being generated after ring-opening with MeOH to give stereodefined dihydropyranones with excellent stereocontrol (10 examples, typically ～90 : 10 dr and >95 : 5 er).

A convenient one-pot completely stereoselective synthesis of trans-4-Hydroxystilbenes and its derivatives and X-ray structure of its precursor

The synthesis of E-isomer of 4-Hydroxystilbene and its derivatives 3 by reductive elimination of the carbonyl function in 2-phenyl-1-(4-hydroxyphenyl)ethan-1-one and its derivatives 2 and the X-ray structure of 2a are described.