1325725-59-4

Basic information

• Product Name: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-3,3-dimethyl-1-((R)-2-(9-methyl-9H-carbazol-4-yl)pyrrolidin-1-yl)-1-oxobutan-2-yl)thiourea
• Synonyms: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-3,3-dimethyl-1-((R)-2-(9-methyl-9H-carbazol-4-yl)pyrrolidin-1-yl)-1-oxobutan-2-yl)thiourea
• CAS NO: 1325725-59-4
• Molecular Weight: 634.689
• Mol File: 1325725-59-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-3,3-dimethyl-1-((R)-2-(9-methyl-9H-carbazol-4-yl)pyrrolidin-1-yl)-1-oxobutan-2-yl)thiourea(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-3,3-dimethyl-1-((R)-2-(9-methyl-9H-carbazol-4-yl)pyrrolidin-1-yl)-1-oxobutan-2-yl)thiourea(1325725-59-4)
• EPA Substance Registry System: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-3,3-dimethyl-1-((R)-2-(9-methyl-9H-carbazol-4-yl)pyrrolidin-1-yl)-1-oxobutan-2-yl)thiourea(1325725-59-4)

Safety Data

• Hazardous Substances Data: 1325725-59-4(Hazardous Substances Data)

Upstream product

• 244205-40-1 (2-bromophenyl)boronic acid 
• 17613-47-7 2-bromo-2′-nitro-1,1′-biphenyl 
• 609-73-4 o-nitroiodobenzene 
• 62965-35-9 N-tert-butyloxycarbonyl-L-tert-leucine 
• 3652-89-9 4-bromo-9H-carbazole 
• 1325725-80-1 (S)-3,3-dimethyl-1-((R)-2-(9-methyl-9H-carbazol-4-yl)pyrrolidin-1-yl)-1-oxobutan-2-aminium chloride 
• 23165-29-9 3,5-bistrifluoromethylphenylisothiocyanate 
• 1325725-78-7 tert-butyl (S)-3,3-dimethyl-1-((R)-2-(9-methyl-9H-carbazol-4-yl)pyrrolidin-1-yl)-1-oxobutan-2-ylcarbamate 
• 1325725-79-8 (R)-2-(9-methyl-9H-carbazol-4-yl)pyrrolidinium chloride 
• 1325725-77-6 (R)-tert-butyl 2-(9-methyl-9H-carbazol-4-yl)pyrrolidine-1-carboxylate 

Relevant articles and documents

Enantioselective acylation of silyl ketene acetals through fluoride anion-binding catalysis

A highly enantioselective acylation of silyl ketene acetals with acyl fluorides has been developed to generate useful α,α-disubstituted butyrolactone products. This transformation is promoted by a new thiourea catalyst and 4-pyrrolidinopyridine and represents the first example of enantioselective thiourea anion-binding catalysis with fluoride.