60561-74-2

Usage

Uses

Used in Pharmaceutical Industry:
(4-Methoxy-phenylamino)-phenyl-acetic acid is used as a potential therapeutic agent for the treatment of various conditions, such as inflammation and pain. Its unique chemical structure allows it to potentially interact with biological systems and exhibit relevant pharmacological properties.
Further research and development may be needed to fully understand the potential therapeutic benefits of (4-Methoxy-phenylamino)-phenyl-acetic acid and to explore its applications in different industries.

Upstream product

• 7647-01-0 hydrogenchloride 
• 20265-97-8 p-anisidine hydrochloride 
• 4870-65-9 2-bromophenylacetic acid 
• 104-94-9 4-methoxy-aniline 
• 124-38-9 carbon dioxide 
• 100-52-7 benzaldehyde 
• 783-08-4 [4-(benzylideneamino)phenyl]methanol 
• 1033696-64-8 C₂₁H₂₆N₂O₂ 
• 129544-55-4 3-methylidene-4-phenyl-2-azetidinone 
• 94612-33-6 1-(4-methoxyphenyl)-4-phenylazetidine-2,3-dione 
• 32323-74-3 2-(4-methyloxyphenylamino)-2-phenylacetonitrile 

Downstream Products

• 68150-25-4 3-(4-methoxy-phenyl)-4-phenyl-2,2-bis-trifluoromethyl-oxazolidin-5-one 
• 24461-61-8 phenylglycine methyl ester 
• 125990-08-1 methyl α-(p-methoxyphenylamino)-α-phenylacetate 
• 68150-37-8 7-diethylamino-3-(4-methoxy-phenyl)-6-methyl-4-phenyl-2,2-bis-trifluoromethyl-3,4-dihydro-2H-[1,3]oxazepin-5-one 

Relevant academic research and scientific papers

Integrated Flow Synthesis of α-Amino Acids byIn SituGeneration of Aldimines and Subsequent Electrochemical Carboxylation

The synthesis of α-amino acids was carried out in a continuous flow system. In this system, aldimines were efficiently generatedin situvia the dehydration-condensation of aldehydes with anilines in a desiccant bed column filled with 4 ? molecular sieves d

Boric acid catalyzed Ugi three-component reaction in aqueous media

B(OH)3 catalyzed Ugi three-component reaction for the synthesis of 2-arylamino-2-phenylacetamide has been developed using aldehydes, amines, and isocyanides in water. The synthesized 2-arylamino-2-phenylacetamides were efficiently converted int

A synthesis of α-amino acids via direct reductive carboxylation of imines with carbon dioxide

A method for the synthesis of α-amino acids by direct reductive carboxylation of aromatic imines with CO2 is described. The protocol employs readily available commercial reagents and serves as a one-step alternative to the Strecker synthesis. The Royal Society of Chemistry 2013.

A novel one-step approach for the preparation of α-amino acids, α-amino amides, and dipeptides from azetidine-2,3-diones

A remarkable reaction of azetidine-2,3-diones with primary as well as secondary amines, and water is presented. Simply by varying the nucleophile, an unprecedented one-step synthesis of α-amino acids, α-amino amides, and dipeptides, was developed in both

Synthesis of Some New 3,4-Diarylsydnones

The synthesis of some new sydnones 4 is described.Their characteristic absorption maxima, mass spectroscopic fragmentation and C=O-valence vibrations are given.The sydnones 4 are synthezid by nitrosation of C,N-diarylglycines 3 (from strecker synthesis) a