940866-95-5

Basic information

• Product Name: ethyl N-phenyl-α-phenylglycinate
• Synonyms: ethyl N-phenyl-α-phenylglycinate
• CAS NO: 940866-95-5
• Molecular Weight: 255.316
• Mol File: 940866-95-5.mol
• Article Data: 21

Chemical Properties

• CAS DataBase Reference: ethyl N-phenyl-α-phenylglycinate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl N-phenyl-α-phenylglycinate(940866-95-5)
• EPA Substance Registry System: ethyl N-phenyl-α-phenylglycinate(940866-95-5)

Safety Data

• Hazardous Substances Data: 940866-95-5(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 3684-12-6 2-phenyl-2-(phenylamino)acetic acid 
• 62-53-3 aniline 
• 2882-19-1 ethyl 2-phenyl-2-bromoacetate 
• 2556-46-9 N,N'-diphenylbenzamidine 
• 75-00-3 chloroethane 
• 124-38-9 carbon dioxide 
• 538-51-2 benzylidene phenylamine 
• 19078-72-9 bromo(phenyl)acetyl chloride 
• 22065-57-2 ethyl 2-phenyldiazoacetate 
• 101-97-3 Ethyl 2-phenylethanoate 
• 623-73-4 diazoacetic acid ethyl ester 
• 591-50-4 iodobenzene 
• 586-96-9 Nitrosobenzene 

Downstream Products

• 93-89-0 benzoic acid ethyl ester 
• 99365-60-3 1-phenyl-1-(phenylamino)octan-2-one 
• 106989-73-5 1-phenyl-1-(phenylamino)propan-2-one 
• 5722-91-8 1,2-diphenyl-2-(phenylamino)ethanone 
• 1360998-10-2 1,4,5-triphenyl-1H-imidazol-2-amine 
• 1360998-09-9 4-hexyl-1,5-diphenyl-1H-imidazol-2-amine 
• 1360998-08-8 4-methyl-1,5-diphenyl-1H-imidazol-2-amine 
• 81278-20-8 1,5-diphenyl-2--3,4-bis(carbomethoxy)pyrrole 
• 81278-17-3 N-phenyl-N--2-phenylglycine 
• 66380-05-0 (N-acetyl-anilino)-phenyl-acetic acid 
• 81278-18-4 [(2-But-3-enyl-4-methoxy-benzoyl)-phenyl-amino]-phenyl-acetic acid ethyl ester 
• 66380-15-2 2-methyl-5-methylsulfanyl-3,4-diphenyl-thiazolium; iodide 
• 66380-18-5 acetic (5-acetylsulfanyl-3,4-diphenyl-3H-thiazol-2-ylidene)-thioacetic thioanhydride 
• 66380-12-9 2-methyl-3,4-diphenyl-5-thioxo-4,5-dihydro-thiazolium betaine 

Relevant articles and documents

Method for realizing insertion reaction of diazo ester compound and aniline molecule N-H through photocatalytic micro-channel

A homogeneous solution containing the aniline represented by the formula N, a derivative thereof and a diazo ester compound shown H is pumped into a microchannel reaction device with a light source to react to obtain I phenyl II benzene ethyl acetate deri

Method for constructing C-N bond through insertion reaction of non-metal catalyzed sulfur ylide and aromatic amine and application

The invention relates to a method for constructing a C-N bond through an insertion reaction of non-metal catalyzed sulfur ylide and aromatic amine and application. According to the method, water is used as a reaction solvent, and sulfur ylide is subjected to an N-H insertion reaction under mild conditions to construct a C-N bond. As a way of constructing a C-N bond, the method overcomes the defects of traditional use of metal catalysts or oxidants. On the basis of the method, various alpha-amino acid ester derivatives can be obtained by using different aromatic amines as substrates. Accordingto the method, the raw materials are easy to obtain, use of a metal catalyst, an oxidizing agent and an organic solvent is avoided, and the method is a mild, effective and environment-friendly methodfor preparing the alpha-amino acid ester and has wide application prospects.

Carbene X[sbnd]H bond insertions catalyzed by copper(I) macrocyclic pyridine-containing ligand (PcL) complexes

A catalytic system comprising copper(I) and macrocyclic pyridine-containing ligands (Pc-L) proves capable of promoting carbene Si[sbnd]H bond insertions using diazo compounds as the carbene source. This catalytic system showed broad scope and a remarkable robustness as indicated by high TON numbers (up to 30000). Moreover, the use of enynones as carbene sources proved also feasible in hydrosilane insertion using this catalytic system. Finally, the insertion in O[sbnd]H and N[sbnd]H bonds of phenols and anilines, respectively, has been also demonstrated.