93593-09-0

Basic information

• Product Name: (2-Fluoro-phenyl)-[2-(1-methyl-piperidin-4-ylamino)-phenyl]-methanone
• CAS NO: 93593-09-0
• Molecular Weight: 312.387
• Mol File: 93593-09-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2-Fluoro-phenyl)-[2-(1-methyl-piperidin-4-ylamino)-phenyl]-methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2-Fluoro-phenyl)-[2-(1-methyl-piperidin-4-ylamino)-phenyl]-methanone(93593-09-0)
• EPA Substance Registry System: (2-Fluoro-phenyl)-[2-(1-methyl-piperidin-4-ylamino)-phenyl]-methanone(93593-09-0)

Safety Data

• Hazardous Substances Data: 93593-09-0(Hazardous Substances Data)

Upstream product

• 22261-94-5 N-(1-methyl-4-piperidinyl)aniline 
• 394-47-8 2-fluorobenzonitrile 
• 62-53-3 aniline 
• 1445-73-4 1-Methyl-4-piperidone 

Downstream Products

• 93592-02-0 4-{[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-acetyl]-[2-(2-fluoro-benzoyl)-phenyl]-amino}-piperidine-1-carboxylic acid benzyl ester 
• 93592-15-5 4-[3-Acetoxy-5-(2-fluoro-phenyl)-2-oxo-2,3-dihydro-benzo[e][1,4]diazepin-1-yl]-piperidine-1-carboxylic acid benzyl ester 
• 93592-14-4 4-[5-(2-Fluoro-phenyl)-2-oxo-4-oxy-2,3-dihydro-benzo[e][1,4]diazepin-1-yl]-piperidine-1-carboxylic acid benzyl ester 
• 93592-03-1 4-[5-(2-Fluoro-phenyl)-2-oxo-2,3-dihydro-benzo[e][1,4]diazepin-1-yl]-piperidine-1-carboxylic acid benzyl ester 
• 93592-01-9 4-[2-(2-Fluoro-benzoyl)-phenylamino]-piperidine-1-carboxylic acid benzyl ester 
• 93592-13-3 1,3-dihydro-5-(2-fluorophenyl)-1-(1-methyl-4-piperidinyl)-7-nitro-2H-1,4-benzodiazepin-2-one 
• 93592-16-6 1,3-dihydro-5-(2-fluorophenyl)-3-hydroxy-1-(4-piperidinyl)-2H-1,4-benzodiazepin-2-one 
• 93592-73-5 1,3-dihydro-5-(2-fluorophenyl)-1-(1-methyl-4-piperidinyl)-2H-1,4-benzodiazepin-2-one 
• 93592-04-2 5-(2-Fluoro-phenyl)-1-piperidin-4-yl-1,3-dihydro-benzo[e][1,4]diazepin-2-one 
• 96110-86-0 (2-Fluoro-phenyl)-[2-(piperidin-4-ylamino)-phenyl]-methanone 
• 93591-99-2 4-[2-(2-Fluoro-benzoyl)-phenylamino]-piperidine-1-carboxylic acid ethyl ester 

Relevant articles and documents

Aminohaloborane in Organic Synthesis. IX. Exclusive ortho Acylation Reaction of N-Monoaminoalkylanilines

The exclusive ortho acylation reaction of aniline derivatives using boron trichloride made possible the one-step synthesis of 2-acyl-N-monoaminoalkylanilines (1) and the corresponding imines (2) from N-monoaminoalkylanilines, even in the case of compounds with a bulky substituent at the nitrogen atom.Conventional methods only give 1 via elaborate procedures.Keywords: regioselective reaction; 2-acylaniline derivative; 2-acylaniline-imine derivative; boron trichloride