489453-01-2

Basic information

• Product Name: Carbamic acid, [4-[3-[4-[[(1,1-dimethylethoxy)carbonyl](phenylmethoxy)amino]butyl]tetra hydro-2,4,6-trioxo-1,3,5-triazin-1(2H)-yl]butyl](phenylmethoxy)-, 2,2,2-trichloroethyl ester
• CAS NO: 489453-01-2
• Molecular Formula: C33H42Cl3N5O9
• Molecular Weight: 759.084
• Mol File: 489453-01-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [4-[3-[4-[[(1,1-dimethylethoxy)carbonyl](phenylmethoxy)amino]butyl]tetra hydro-2,4,6-trioxo-1,3,5-triazin-1(2H)-yl]butyl](phenylmethoxy)-, 2,2,2-trichloroethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [4-[3-[4-[[(1,1-dimethylethoxy)carbonyl](phenylmethoxy)amino]butyl]tetra hydro-2,4,6-trioxo-1,3,5-triazin-1(2H)-yl]butyl](phenylmethoxy)-, 2,2,2-trichloroethyl ester(489453-01-2)
• EPA Substance Registry System: Carbamic acid, [4-[3-[4-[[(1,1-dimethylethoxy)carbonyl](phenylmethoxy)amino]butyl]tetra hydro-2,4,6-trioxo-1,3,5-triazin-1(2H)-yl]butyl](phenylmethoxy)-, 2,2,2-trichloroethyl ester(489453-01-2)

Safety Data

• Hazardous Substances Data: 489453-01-2(Hazardous Substances Data)

Upstream product

• 27738-96-1 chlorocarbonyl isocyanate 
• 489452-98-4 1-[4-[N-(trichloroethoxycarbonyl)benzyloxyamino]butyl]-3-[4-[N-(tert-butyloxycarbonyl)benzyloxyamino]butyl]urea 
• 489452-97-3 5-[N-(trichloroethoxycarbonyl)benzyloxyamino]pentanoic acid 
• 489452-96-2 5-[N-(trichloroethoxycarbonyl)benzyloxyamino]pentanoic acid methyl ester 
• 1027408-37-2 4-[N-(tert-butyloxycarbonyl)benzyloxyamino]-1-butylamine 
• 489452-95-1 4-[N-(tert-butyloxycarbonyl)benzyloxyamino]butyronitrile 
• 79722-21-7 tert-butyl N-(benzyloxy)carbamate 
• 90195-00-9 N-<(2,2,2-trichloroethoxy)carbonyl>-O-benzylhydroxylamine 

Relevant articles and documents

The preparation of a fully differentiated "multiwarhead" siderophore precursor

A protected, fully differentiated siderophore analogue has been prepared so that "Trojan Horse"-like siderophore drug conjugates with different drugs can be synthesized. The key steps in the synthesis include controlled preparation of an unsymmetrical urea and its conversion to a fully differentiated isocyanurate by reaction with chloro(carbonyl) isocyanate.