1374982-07-6

Basic information

• Product Name: (R)-2-{3-[benzyl-(2,2-dimethoxyethyl)amino]-2-hydroxypropyl}-1H-isoindole-1,3(2H)-dione
• CAS NO: 1374982-07-6
• Molecular Weight: 398.459
• Mol File: 1374982-07-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-2-{3-[benzyl-(2,2-dimethoxyethyl)amino]-2-hydroxypropyl}-1H-isoindole-1,3(2H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-{3-[benzyl-(2,2-dimethoxyethyl)amino]-2-hydroxypropyl}-1H-isoindole-1,3(2H)-dione(1374982-07-6)
• EPA Substance Registry System: (R)-2-{3-[benzyl-(2,2-dimethoxyethyl)amino]-2-hydroxypropyl}-1H-isoindole-1,3(2H)-dione(1374982-07-6)

Safety Data

• Hazardous Substances Data: 1374982-07-6(Hazardous Substances Data)

Upstream product

• 54879-88-8 N-benzyl-2,2-dimethoxyethylamine 
• 161596-47-0 (S)-N-glycidylphthalimide 

Downstream Products

• 1374982-08-7 (2R,6S)-2-[(4-benzyl-6-methoxymorpholin-2-yl)methyl]-1H-isoindole-1,3(2H)-dione 
• 1374982-09-8 (2R,6R)-2-[(4-benzyl-6-methoxymorpholin-2-yl)methyl]-1H-isoindole-1,3(2H)-dione 

Relevant articles and documents

Stereocontrolled access to optically-enriched oxabispidines

A range of chiral, optically-enriched bicyclic oxabispidines were prepared from (S)-(-)-2,3-epoxypropylphthalimide using an efficient sequence featuring a stereocontrolled intramolecular Mannich reaction as the key transformation.