211430-93-2

Basic information

• Product Name: Ethyl 2-benzyl-3-oxoisoindoline-1-carboxylate
• Synonyms: Ethyl 2-benzyl-3-oxoisoindoline-1-carboxylate
• CAS NO: 211430-93-2
• Molecular Formula: C₁₈H₁₇NO₃
• Molecular Weight: 295.33248
• Mol File: 211430-93-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ethyl 2-benzyl-3-oxoisoindoline-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 2-benzyl-3-oxoisoindoline-1-carboxylate(211430-93-2)
• EPA Substance Registry System: Ethyl 2-benzyl-3-oxoisoindoline-1-carboxylate(211430-93-2)

Safety Data

• Hazardous Substances Data: 211430-93-2(Hazardous Substances Data)

Upstream product

• 14961-34-3 diethyl homophthalate 
• 79016-11-8 ethyl 2-(1-bromo-2-ethoxy-2-oxoethyl)benzoate 
• 100-46-9 benzylamine 

Downstream Products

• 1451076-21-3 C₂₁H₁₆N₂O₃ 
• 1451076-17-7 2'-(4-methoxybenzyl)-6-vinyl-8,8a-dihydro-2H-spiro[indolizine-1,1'-isoindoline]-3,3'(5H)-dione 

Relevant articles and documents

A systematic study on the use of different organocatalytic activation modes for asymmetric conjugated addition reactions of isoindolinones

In this article we describe a series of new asymmetric Michael reactions of carboxylate-3-substituted isoindolinones used as nucleophiles in the synthesis of valuable chiral tetrasubstituted derivatives. It has been shown that the reactivity and enantiose

Halolactonization of γ-acetylenic acids: systhesis of novel spiroisoindole halobutyrolactones

γ-Acetylenic carboxylic acids are cyclized to spirohalo butyrolactones, in the presence of NBS or NIS and K2CO3. The corresponding 5(E)-haloalkylidene-spirobutyrolactones were isolated in high yields, and this process constitutes an easy and efficient route to analogous structures of natural products of biological interest.