1027408-37-2

Basic information

• Product Name: 4-[N-(tert-butyloxycarbonyl)benzyloxyamino]-1-butylamine
• Synonyms: 4-[N-(tert-butyloxycarbonyl)benzyloxyamino]-1-butylamine
• CAS NO: 1027408-37-2
• Molecular Weight: 294.394
• Mol File: 1027408-37-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-[N-(tert-butyloxycarbonyl)benzyloxyamino]-1-butylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[N-(tert-butyloxycarbonyl)benzyloxyamino]-1-butylamine(1027408-37-2)
• EPA Substance Registry System: 4-[N-(tert-butyloxycarbonyl)benzyloxyamino]-1-butylamine(1027408-37-2)

Safety Data

• Hazardous Substances Data: 1027408-37-2(Hazardous Substances Data)

Upstream product

• 79722-21-7 tert-butyl N-(benzyloxy)carbamate 
• 489452-95-1 4-[N-(tert-butyloxycarbonyl)benzyloxyamino]butyronitrile 

Downstream Products

• 489452-98-4 1-[4-[N-(trichloroethoxycarbonyl)benzyloxyamino]butyl]-3-[4-[N-(tert-butyloxycarbonyl)benzyloxyamino]butyl]urea 
• 489453-01-2 1-[4-[N-(trichloroethoxycarbonyl)benzyloxyamino]butyl]-3-[4-[N-(tert-butyloxycarbonyl)benzyloxyamino]butyl][1.3.5]triazinane-2,4,6-trione 

Relevant articles and documents

Identification of a gene cluster that directs putrebactin biosynthesis in Shewanella species: PubC catalyzes cyclodimerization of N-Hydroxy-N- succinylputrescine

Putrebactin is a dihydroxamate iron chelator produced by the metabolically versatile marine bacterium Shewanella putrefaciens. It is a macrocyclic dimer of N-hydroxy-N-succinyl-putrescine (HSP) and is structurally related to desferrioxamine E, which is a

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.