957770-67-1

Basic information

• Product Name: N-[3,5-bis(trifluoroMethyl)phenyl]-N'-(8α,9S)-cinchonan-9-yl-Urea
• Synonyms: N-[3,5-bis(trifluoroMethyl)phenyl]-N'-(8α,9S)-cinchonan-9-yl-Urea
• CAS NO: 957770-67-1
• Molecular Weight: 0
• Mol File: 957770-67-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-[3,5-bis(trifluoroMethyl)phenyl]-N'-(8α,9S)-cinchonan-9-yl-Urea(CAS DataBase Reference)
• NIST Chemistry Reference: N-[3,5-bis(trifluoroMethyl)phenyl]-N'-(8α,9S)-cinchonan-9-yl-Urea(957770-67-1)
• EPA Substance Registry System: N-[3,5-bis(trifluoroMethyl)phenyl]-N'-(8α,9S)-cinchonan-9-yl-Urea(957770-67-1)

Safety Data

• Hazardous Substances Data: 957770-67-1(Hazardous Substances Data)

Upstream product

• 118-10-5 cinchonidine 
• 779974-91-3 C₁₉H₂₃N₃ 
• 16588-74-2 3,5-ditrifluoromethylisocyanate 
• 485-71-2 Cinchonidin 
• 1263486-03-8 9-amino(9-deoxy)epicinchonidine triple hydrochloride salt 

Relevant articles and documents

Total synthesis of (-)-nakadomarin A

A highly diastereoselective bifunctional organocatalyst controlled Michael addition, a nitro-Mannich/lactamization cascade, a furan N-acyliminium cyclisation, a sequential alkyne RCM/syn-reduction and an alkene RCM has allowed a 19 step, highly stereosele

Asymmetric indoline synthesis via intramolecular aza-Michael addition mediated by bifunctional organocatalysts

A novel method for the asymmetric synthesis of 2-substituted indolines, employing bifunctional amino(thio)urea catalysts, was developed. The reaction proceeded via an intramolecular aza-Michael addition mediated by activation through hydrogen bonding. The