28172-56-7

Basic information

• Product Name: 2-(4-chlorobenzamido)-2-phenylacetic acid
• Synonyms: 2-(4-chlorobenzamido)-2-phenylacetic acid
• CAS NO: 28172-56-7
• Molecular Weight: 289.718
• Mol File: 28172-56-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(4-chlorobenzamido)-2-phenylacetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-chlorobenzamido)-2-phenylacetic acid(28172-56-7)
• EPA Substance Registry System: 2-(4-chlorobenzamido)-2-phenylacetic acid(28172-56-7)

Safety Data

• Hazardous Substances Data: 28172-56-7(Hazardous Substances Data)

Upstream product

• 122-01-0 4-chloro-benzoyl chloride 
• 2835-06-5 phenylglycin 

Downstream Products

• 1426830-22-9 ethyl 2-(4-chlorophenyl)-4-phenyl-1H-imidazole-5-carboxylate 
• 1261646-86-9 C₂₂H₁₈ClNO₃ 
• 106986-07-6 2-(4-Chloro-phenyl)-4-phenyl-2-(3-phenyl-prop-2-ynyl)-2H-oxazol-5-one 
• 106985-95-9 2-(4-Chloro-phenyl)-4-phenyl-4-(1-phenyl-propa-1,2-dienyl)-4H-oxazol-5-one 
• 106985-93-7 2-(4-Chloro-phenyl)-4-phenyl-4-propa-1,2-dienyl-4H-oxazol-5-one 
• 17629-27-5 3-methyl-5-p-chlorophenyl-1-hydropyrazole 
• 107914-74-9 (E)-2-(4-Chlorphenyl)-2-(2-methyl-3-phenyl-2-propenyl)-4-phenyl-5(2H)-oxazolon 
• 911106-53-1 2-fluoro-1-heptylprop-2-enyl [(4-chlorobenzoyl)amino](phenyl)acetate 
• 106985-85-7 propargyl N-(4-chlorobenzoyl)-C-phenylglycinate 
• 107914-69-2 (E)-N-(4-Chlorbenzoyl)-DL-2-phenylglycin-2-methyl-3-phenyl-2-propenylester 
• 104091-16-9 (Z,E)-2-(4-Chlorphenyl)-2-(2,4-hexadienyl)-4-phenyl-5(2H)-oxazolon 
• 104091-12-5 (E,E)-2-(4-Chlorphenyl)-2-(2,4-hexadienyl)-4-phenyl-5(2H)-oxazolon 
• 104091-13-6 2-(4-Chlorphenyl)-3a,6a-dihydro-6a-phenyl-4-(1-propenyl)-3H-furo<3,4-b>pyrrol-6(4H)-on 
• 106985-87-9 (4-Chloro-benzoylamino)-phenyl-acetic acid 3-phenyl-prop-2-ynyl ester 

Relevant articles and documents

Enantioselective iridium catalyzed α-alkylation of azlactones by a tandem asymmetric allylic alkylation/aza-Cope rearrangement

The development of an iridium catalyzed enantioselective α-alkylation of azlactones has been described. The reaction provides rapid access to a wide range of enantio-enriched quaternary carbon center allylated 2,4-diaryloxazol-5(2H)-ones in excellent yiel