1609261-66-6

Basic information

• Product Name: (R)-tert-butyl 3-benzyl-3-((S)-1-(3,4-dichlorophenyl)-2-nitroethyl)-2-oxoindoline-1-carboxylate
• Synonyms: (R)-tert-butyl 3-benzyl-3-((S)-1-(3,4-dichlorophenyl)-2-nitroethyl)-2-oxoindoline-1-carboxylate
• CAS NO: 1609261-66-6
• Molecular Weight: 541.431
• Mol File: 1609261-66-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-tert-butyl 3-benzyl-3-((S)-1-(3,4-dichlorophenyl)-2-nitroethyl)-2-oxoindoline-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-tert-butyl 3-benzyl-3-((S)-1-(3,4-dichlorophenyl)-2-nitroethyl)-2-oxoindoline-1-carboxylate(1609261-66-6)
• EPA Substance Registry System: (R)-tert-butyl 3-benzyl-3-((S)-1-(3,4-dichlorophenyl)-2-nitroethyl)-2-oxoindoline-1-carboxylate(1609261-66-6)

Safety Data

• Hazardous Substances Data: 1609261-66-6(Hazardous Substances Data)

Upstream product

• 862907-10-6 tert-butyl 3-benzyl-2-oxoindoline-1-carboxylate 
• 37630-23-2 1,2-dichloro-4-(2-nitrovinyl)benzene 

Relevant articles and documents

Novel tartrate-derived guanidine-catalyzed highly enantio- and diastereoselective Michael addition of 3-substituted oxindoles to nitroolefins

The Michael addition of 3-substituted oxindoles to nitroolefins was catalyzed by a novel tartrate-derived guanidine in high yield with excellent diastereo- and enantioselectivity. This method showed an extraordinarily broad substrate scope in terms of both reaction partners. the Partner Organisations 2014.