60561-74-2

Basic information

• Product Name: (4-METHOXY-PHENYLAMINO)-PHENYL-ACETIC ACID
• Synonyms: (4-METHOXY-PHENYLAMINO)-PHENYL-ACETIC ACID
• CAS NO: 60561-74-2
• Molecular Formula: C₁₅H₁₅NO₃
• Molecular Weight: 257.28
• Mol File: 60561-74-2.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (4-METHOXY-PHENYLAMINO)-PHENYL-ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (4-METHOXY-PHENYLAMINO)-PHENYL-ACETIC ACID(60561-74-2)
• EPA Substance Registry System: (4-METHOXY-PHENYLAMINO)-PHENYL-ACETIC ACID(60561-74-2)

Safety Data

• Hazardous Substances Data: 60561-74-2(Hazardous Substances Data)

Usage

General Description

(4-Methoxy-phenylamino)-phenyl-acetic acid is a chemical compound with potential pharmaceutical applications. It is a derivative of phenylacetic acid and contains a methoxy group and an amino group attached to the phenyl ring. (4-METHOXY-PHENYLAMINO)-PHENYL-ACETIC ACID has been studied for its potential use in the treatment of various conditions, such as inflammation and pain. Its chemical structure suggests that it may have the ability to 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.

Upstream product

• 32323-74-3 2-(4-methyloxyphenylamino)-2-phenylacetonitrile 
• 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 
• 20265-97-8 p-anisidine hydrochloride 
• 129544-55-4 3-methylidene-4-phenyl-2-azetidinone 
• 94612-33-6 1-(4-methoxyphenyl)-4-phenylazetidine-2,3-dione 
• 7647-01-0 hydrogenchloride 

Downstream Products

• 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 
• 68150-25-4 3-(4-methoxy-phenyl)-4-phenyl-2,2-bis-trifluoromethyl-oxazolidin-5-one 

Relevant articles and documents

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

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