186685-89-2

Usage

Uses

Used in Pharmaceutical Industry:
2-(4-Formyl-2-methoxy-phenoxy)-acetamide is used as a key intermediate in the synthesis of various pharmaceuticals for its unique chemical properties and reactivity. It plays a crucial role in the development of new drugs and medicinal compounds, contributing to advancements in healthcare and medicine.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(4-Formyl-2-methoxy-phenoxy)-acetamide is utilized as a versatile building block for the creation of a wide range of organic compounds. Its distinct structure and functional groups enable chemists to explore various synthetic pathways and reactions, leading to the formation of novel and useful molecules.
Used in Research and Development:
2-(4-Formyl-2-methoxy-phenoxy)-acetamide is employed as a valuable research tool in academic and industrial laboratories. Its unique chemical characteristics and reactivity make it an interesting subject for studying various chemical reactions, mechanisms, and processes. 2-(4-FORMYL-2-METHOXY-PHENOXY)-ACETAMIDE contributes to the expansion of scientific knowledge and the development of innovative applications in the chemical and related industries.

InChI:InChI=1/C10H11NO4/c1-14-9-4-7(5-12)2-3-8(9)15-6-10(11)13/h2-5H,6H2,1H3,(H2,11,13)

Upstream product

• 121-33-5 vanillin 
• 79-07-2 Chloroacetamide 

Downstream Products

• 554402-60-7 3-amino-3-(4-carbamoylmethoxy-3-methoxy-phenyl)-propionic acid 
• 340812-14-8 2-[4-(2-amino-3-cyano-5-oxo-4H,5H-pyrano[3,2-c]chromen-4-yl)-2-methoxy-phenoxy]-acetamide 

Relevant academic research and scientific papers

Alkylation of NH-, OH-, and SH-acids in the presence of potassium carbonate: 1. Functionalization of chloromethyl group of alkoxy-substituted aromatic aldehydes

An easily scalable, economocal, and more safe method for the preparation of 3-chloromethyl-4-methoxybenzaldehyde was developed. The latter was subjected to reactions with NH-, OH-, and SH-acids in the presence of potassium carbonate to obtain new aromatic aldehydes in high yields.

Structure-activity relationships and molecular modelling of new 5-arylidene-4-thiazolidinone derivatives as aldose reductase inhibitors and potential anti-inflammatory agents

A series of 5-(carbamoylmethoxy)benzylidene-2-oxo/thioxo-4-thiazolidinone derivatives (6-9) were synthesized as inhibitors of aldose reductase (AR), enzyme which plays a crucial role in the development of diabetes complications as well as in the inflammat

Competitive formation of β-amino acids, propenoic, and ylidenemalonic acids by the Rodionov reaction from malonic acid, aldehydes, and ammonium acetate in alcoholic medium

The Rodionov reaction of 49 available aliphatic and aromatic aldehydes with malonic acid and ammonium acetate in alcoholic medium, resulting in formation of β-amino acids, propenoic, and ylidenemalonic acids, was studied. Certain regioselectivity regularities of the reaction were revealed. Among the variety of ketones studied, cyclohexanone is the only whose reaction yields a β-amino acid. Unusual dehydrofluorination of 6-chloro-2-fluorocinnamic acid under the Rodionov reaction was discovered. 2005 Pleiades Publishing, Inc.