73190-70-2

Basic information

• Product Name: N-(2-NAPHTHYL)-2-PHENYLACETAMIDE
• Synonyms: N-(2-NAPHTHYL)-2-PHENYLACETAMIDE
• CAS NO: 73190-70-2
• Molecular Formula: C₁₈H₁₅NO
• Molecular Weight: 0
• Mol File: 73190-70-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 513.3°C at 760 mmHg
• Flash Point: 308.6°C
• Appearance: /
• Density: 1.202g/cm³
• Vapor Pressure: 1.2E-10mmHg at 25°C
• Refractive Index: 1.687
• CAS DataBase Reference: N-(2-NAPHTHYL)-2-PHENYLACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-NAPHTHYL)-2-PHENYLACETAMIDE(73190-70-2)
• EPA Substance Registry System: N-(2-NAPHTHYL)-2-PHENYLACETAMIDE(73190-70-2)

Safety Data

• Hazardous Substances Data: 73190-70-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C18H15NO/c20-18(12-14-6-2-1-3-7-14)19-17-11-10-15-8-4-5-9-16(15)13-17/h1-11,13H,12H2,(H,19,20)

Upstream product

• 103-82-2 phenylacetic acid 
• 91-59-8 naphthalen-2-ylamine 
• 454713-45-2 naphthalen-2-yl-carbamic acid tert-butyl ester 
• 103-83-3 N,N'-dimethylbenzylamine 
• 260783-80-0 N,N,N--trimethyl--1--phenylmethanaminium trifluoromethanesulfonate 
• 201230-82-2 carbon monoxide 

Downstream Products

• 115916-74-0 N,N'-di-[2]naphthyl-2-phenyl-acetamidine 
• 22440-24-0 3-benzyl-2H-benzo[f]quinazolin-1-one 

Relevant articles and documents

Palladium-catalyzed carbonylation of benzylic ammonium salts to amides and esters: Via C-N bond activation

An efficient palladium-catalyzed carbonylation reaction of readily available quaternary ammonium salts with CO is reported for the first time to afford arylacetamides and arylacetic acid esters via benzylic C-N bond cleavage. This protocol features mild reaction conditions under atmospheric pressure of CO, a redox-neutral process without an additional oxidant, and a broad substrate scope for various kinds of amines, alcohols and phenols.

Triethyl phosphite-p-dimethylaminopyridine, a new reagent for direct syntheses of amides from aliphatic carboxylic acids and amines

Various amides have been prepared with high to moderate yields from the corresponding aliphatic carboxylic acids and amines using triethyl phosphite-p-dimethylaminopyridine as a new reagent and pyridine as solvent, at 100-110°C, for 12 hours.