1197208-65-3

Basic information

• Product Name: C₂₈H₂₉N₃O₅
• Synonyms: C₂₈H₂₉N₃O₅
• CAS NO: 1197208-65-3
• Molecular Weight: 487.555
• Mol File: 1197208-65-3.mol

Chemical Properties

• CAS DataBase Reference: C₂₈H₂₉N₃O₅(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₈H₂₉N₃O₅(1197208-65-3)
• EPA Substance Registry System: C₂₈H₂₉N₃O₅(1197208-65-3)

Safety Data

• Hazardous Substances Data: 1197208-65-3(Hazardous Substances Data)

Upstream product

• 36208-62-5 1,3-dibenzyl-1,3-dihydroindol-2-one 
• 1972-28-7 diethylazodicarboxylate 

Relevant articles and documents

New polymer-supported mono- And bis-cinchona alkaloid derivatives: Synthesis and use in asymmetric organocatalyzed reactions

The straightforward synthesis of polystyrene-supported Chinchona alkaloids and their application in the asymmetric dimerization of ketenes is reported. Six different immobilized derivatives, consisting of three dimeric and two monomeric 9-O ethers, were p

Long-Lived Polymer-Supported Dimeric Cinchona Alkaloid Organocatalyst in the Asymmetric α-Amination of 2-Oxindoles

Nearly quantitative yields and high enantiomeric purity (89-95% ee) were attained in the course of 100 reaction cycles of a polystyrene resin-supported Cinchona alkaloid organocatalyst in the enantioselective α-amination of 2-oxindoles with diethyl azodicarboxylate. The catalytic material proved stable for >5300 h operation time over 8 months.

Expanding the scope of cinchona alkaloid-catalyzed enantioselective α-aminations of oxindoles: A versatile approach to optically active 3-amino-2-oxindole derivatives

(Chemical Equation Presented) A cinchona alkaloid-catalyzed, highly enantioselective, α-amination of oxindoles has been developed. The reaction is general, operationally simple, and affords the desired products in high yields with good to excellent enanti