78350-37-5

Basic information

• Product Name: 1-(2-(isopropylamino)phenyl)ethan-1-one
• Synonyms: 1-(2-(isopropylamino)phenyl)ethan-1-one
• CAS NO: 78350-37-5
• Molecular Weight: 177.246
• Mol File: 78350-37-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(2-(isopropylamino)phenyl)ethan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-(isopropylamino)phenyl)ethan-1-one(78350-37-5)
• EPA Substance Registry System: 1-(2-(isopropylamino)phenyl)ethan-1-one(78350-37-5)

Safety Data

• Hazardous Substances Data: 78350-37-5(Hazardous Substances Data)

Upstream product

• 118-93-4 o-hydroxyacetophenone 
• 75-31-0 isopropylamine 
• 75-30-9 2-iodo-propane 
• 551-93-9 2-aminoacetophenone 

Downstream Products

• 1429308-40-6 N-isopropyl-2-(prop-1-en-2-yl)benzenamine 
• 528856-12-4 N-(2-acetylphenyl)-2,2,2-trichloro-N-isopropylacetamide 

Relevant articles and documents

Diastereoselective synthesis of dihydro-quinolin-4-ones by a borane-catalyzed redox-neutral endo-1,7-hydride shift

The borane-catalyzed synthesis of dihydroquinoline-4-ones is developed. The amino-substituted chalcones undergo a 1,7-hydride shift upon Lewis acid activation to form a zwitterionic iminium enolate, which collapses to the dihydroquinoline-4-one scaffold.

Electrosynthesis of 3-chloro-1,4-disubstituted-2(1H)-quinolinones and 3,3-dichloro-4-hydroxy-1,4-disubstituted-3,4-dihydro-2(1H)-quinolinones, as well as a new convenient process to dioxindoles

Cathodic reduction of N-(2-acyl(or aroyl)phenyl)-2,2,2,-trichloro-N-alkylacetamide at - 1.2 V (vs SCE) under aprotic conditions yields 3-chloro-1,4-disubstituted-2(1H)-quinolinones (1) as the major product. When the reaction is carried out at -0.8 V (vs S