315179-49-8

Basic information

• Product Name: Benzoic acid, 2-(diphenylamino)-, methyl ester
• CAS NO: 315179-49-8
• Molecular Formula: C20H17NO2
• Molecular Weight: 303.36
• Mol File: 315179-49-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-(diphenylamino)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-(diphenylamino)-, methyl ester(315179-49-8)
• EPA Substance Registry System: Benzoic acid, 2-(diphenylamino)-, methyl ester(315179-49-8)

Safety Data

• Hazardous Substances Data: 315179-49-8(Hazardous Substances Data)

Upstream product

• 610-94-6 2-bromobenzoic acid methyl ester 
• 122-39-4 diphenylamine 
• 610-97-9 o-iodo-methyl-benzoic acid 
• 108-86-1 bromobenzene 
• 62-53-3 aniline 
• 591-50-4 iodobenzene 
• 67-56-1 methanol 
• 17626-44-7 2-(N,N-diphenylamino)benzoic acid 

Downstream Products

• 855869-14-6 (2-Diphenylamino-phenyl)-diphenyl-methanol 
• 1150-62-5 N-phenylcarbazole 
• 5472-23-1 10-phenylacridin-9(10H)-one 
• 1282540-39-9 C₄₁H₃₂N₄O₈ 
• 1282540-38-8 C₂₀H₂₀N₄O₂ 
• 1282540-37-7 C₂₀H₁₄N₄O₈ 
• 1016163-86-2 methyl 5-iodo-2-[N,N-bis(4-iodophenyl)amino]benzoate 
• 720700-63-0 9,9,10-triphenyl-9,10-dihydro-acridine 
• 315179-51-2 (1R,2R)-2-[N-(2-diphenylaminobenzoyl)amino]cyclohexylcarbamic acid tert-butyl ester 
• 315179-54-5 (1R,2R)-N-(2-amino)cyclohexyl-2-(diphenylamino)benzamide 
• 17626-44-7 2-(N,N-diphenylamino)benzoic acid 

Relevant articles and documents

Redox-neutral decarboxylative photocyclization of anthranilic acids

A mild metal-, catalyst-, and oxidant-free photoredox neutral system has been found to efficiently enable intramolecular decarboxylative cyclization of anthranilic acids. This facile protocol provides an alternative method for the synthesis of carbazoles. Mechanistic studies reveal a key photoinduced 6π-electrocyclization process and formic acid was released as the sole byproduct.

Catalytic Asymmetric Chlorocyclization of 2-Vinylphenylcarbamates for Synthesis of 1,4-Dihydro-2H-3,1-benzoxazin-2-one Derivatives

A facile synthetic approach to a series of chiral 4-chloromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one derivatives has been described. This transformation is achieved through the catalytic asymmetric chlorocyclization of 2-vinylphenylcarbamates using a newly developed organocatalyst. Furthermore, the resulting products can be easily converted into diverse bioactive agents.

Copper-catalyzed synthesis of triarylamines from aryl halides and arylamines

A simple and efficient methodology for the synthesis of triphenylamines has been demonstrated using copper catalyst with a ligand and tripotassium phosphate as the base. The effect of parameters such as catalyst precursors, ligands, bases and solvents were studied and a series of triphenylamines were obtained with moderate to excellent yields in DMF. This reaction displays great functional groups compatibility in the presence of a broad range of functional groups.