1262623-27-7

Basic information

• Product Name: 2-(2-(4-methoxyphenyl)-2-oxoethoxy)isoindoline-1,3-dione
• Synonyms: 2-(2-(4-methoxyphenyl)-2-oxoethoxy)isoindoline-1,3-dione
• CAS NO: 1262623-27-7
• Molecular Weight: 311.294
• Mol File: 1262623-27-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(2-(4-methoxyphenyl)-2-oxoethoxy)isoindoline-1,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-(4-methoxyphenyl)-2-oxoethoxy)isoindoline-1,3-dione(1262623-27-7)
• EPA Substance Registry System: 2-(2-(4-methoxyphenyl)-2-oxoethoxy)isoindoline-1,3-dione(1262623-27-7)

Safety Data

• Hazardous Substances Data: 1262623-27-7(Hazardous Substances Data)

Upstream product

• 637-69-4 4-Methoxystyrene 
• 524-38-9 N-hydroxyphthalimide 

Downstream Products

• 1262623-30-2 C₂₃H₁₉N₃O₄ 
• 136918-14-4 phthalimide 
• 1076-95-5 p-methoxyphenylglyoxal 

Relevant articles and documents

Cobalt Catalyst-Controlled Selective Dioxygenation of Styrenes Using N-Hydroxyphthalimide with Molecular Oxygen

A cobalt-catalyzed selective dioxygenation of styrenes with N-hydroxyphthalimide (NHPI) was developed using molecular oxygen as the terminal oxidant. Alcohol and ketone products can be selectively formed from identical substrates by catalyst control. The reaction was applicable to a broad range of styrenes and exhibited good functional group tolerance. It provided a method for preparation of 1,2-diol or α-hydroxyketone derivatives. (Figure presented.).

Visible-light- induced aerobic dioxygenation of styrenes under metal- and additive-free ambient conditions

Visible light promoted hydroperoxidation of styrenes using hydroxylamine and molecular oxygen from air under metal-free and additive-free conditions at room temperature is described. Hydroperoxides were further converted into corresponding hydroxy compoun

Copper(II)-catalyzed direct dioxygenation of alkenes with air and n -hydroxyphthalimide: Synthesis of β-keto- N -alkoxyphthalimides

Copper(II)-catalyzed direct dioxygenation of alkenes using air and a simple N-hydroxyphthalimide leading to β-keto-N-alkoxyphthalimides has been developed. The reaction system is mild, efficient, and effective at room temperature with broad substrate scope and substantial steric hindrance. The radical-trapping and 18O-labeling experiments have been demonstrated.