130400-06-5

Basic information

• Product Name: C₃₉H₅₅NO₆
• Synonyms: C₃₉H₅₅NO₆
• CAS NO: 130400-06-5
• Molecular Weight: 633.869
• Mol File: 130400-06-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₉H₅₅NO₆(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₉H₅₅NO₆(130400-06-5)
• EPA Substance Registry System: C₃₉H₅₅NO₆(130400-06-5)

Safety Data

• Hazardous Substances Data: 130400-06-5(Hazardous Substances Data)

Upstream product

• 51779-32-9 iminodicarboxylic acid di-tert-butyl ester 
• 115269-99-3 N,N-bis(tert-butoxycarbonyl)allylamine 
• 151283-13-5 Benzoic acid (3S,8R,9S,10S,13S,14S)-10,13-dimethyl-17-trifluoromethanesulfonyloxy-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 

Relevant articles and documents

AN EFFICIENT ROUTE FOR THE STEREOSELECTIVE CONVERSION OF KETONES INTO THREE-CARBONS HOMOLOGATED PRIMARY E-ALLYLAMINES: THE PALLADIUM-CATALYSED REACTION OF VINYL TRIFLATES WITH N,N-DI-TERT-BUTOXYCARBONYL-N-ALLYAMINE.

E-Allylamines N-protected with the easily removable tert-butoxycarbonyl group are stereoselectively prepared in good to high yield through the palladium-catalysed reaction of vinyl triflates with N,N-di-tert-butoxycarbonyl-N-allylamine in the presence of AcOK and n-Bu4NCl.The reaction is very sensitive to the nature of the base.The use of bases other than AcOK has been examined and proved to be unsuccessful.