929206-57-5

Basic information

• Product Name: 1H-Isoindol-1-one, 2,3-dihydro-3-hydroxy-2-[(1S)-1-phenylethyl]-
• CAS NO: 929206-57-5
• Molecular Formula: C16H15NO2
• Molecular Weight: 253.301
• Mol File: 929206-57-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Isoindol-1-one, 2,3-dihydro-3-hydroxy-2-[(1S)-1-phenylethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Isoindol-1-one, 2,3-dihydro-3-hydroxy-2-[(1S)-1-phenylethyl]-(929206-57-5)
• EPA Substance Registry System: 1H-Isoindol-1-one, 2,3-dihydro-3-hydroxy-2-[(1S)-1-phenylethyl]-(929206-57-5)

Safety Data

• Hazardous Substances Data: 929206-57-5(Hazardous Substances Data)

Upstream product

• 85-44-9 phthalic anhydride 
• 3976-26-9 2-((S)-1-phenylethyl)-isoindoline-1,3-dione 

Downstream Products

• 929206-59-7 3-acetoxy-2-(1(S)-phenylethyl)isoindolin-1-one 

Relevant articles and documents

DAST-mediated preparation of N-substituted 3-alkoxyisoindolinones

3-Alkoxy-2-phenylethylisoindolinones are conveniently prepared by reacting the corresponding hydroxylactams with diethylaminosulfur trifluoride (DAST) in the presence of a range of alcohols. The DAST-mediated reaction did not result in any reactant fluori

Intermolecular and intramolecular α-amidoalkylation reactions using bismuth triflate as the catalyst

(Chemical Equation Presented) Bismuth(III) triflate was found to promote the formation of stable cyclic N-acyliminium species in remarkable catalytic amounts (1 mol %). The α-amidoalkylation process seems to be effective in intermolecular and intramolecul