393110-71-9

Basic information

• Product Name: O-(1-(4-(azidomethyl)phenyl)ethyl)-N-(tert-butyl)-N-(2-methyl-1-phenylpropyl)hydroxylamine
• Synonyms: O-(1-(4-(azidomethyl)phenyl)ethyl)-N-(tert-butyl)-N-(2-methyl-1-phenylpropyl)hydroxylamine
• CAS NO: 393110-71-9
• Molecular Weight: 380.533
• Mol File: 393110-71-9.mol

Chemical Properties

• CAS DataBase Reference: O-(1-(4-(azidomethyl)phenyl)ethyl)-N-(tert-butyl)-N-(2-methyl-1-phenylpropyl)hydroxylamine(CAS DataBase Reference)
• NIST Chemistry Reference: O-(1-(4-(azidomethyl)phenyl)ethyl)-N-(tert-butyl)-N-(2-methyl-1-phenylpropyl)hydroxylamine(393110-71-9)
• EPA Substance Registry System: O-(1-(4-(azidomethyl)phenyl)ethyl)-N-(tert-butyl)-N-(2-methyl-1-phenylpropyl)hydroxylamine(393110-71-9)

Safety Data

• Hazardous Substances Data: 393110-71-9(Hazardous Substances Data)

Upstream product

• 227000-85-3 N-tert-butyl-O-[1-(4-chloromethyl-phenyl)-ethyl]-N-(2-methyl-1-phenyl-propyl)-hydroxylamine 

Downstream Products

• 496816-88-7 2,2,5-trimethyl-3-(1'-p-(t-butyloxycarbonylamino)methylphenylethoxy)-4-phenyl-3-azahexane 
• 1616758-34-9 tris((1-(4-(1-((tert-butyl(2-methyl-1-phenylpropyl)amino)oxy)ethyl)benzyl)-1H-1,2,3-triazol-4-yl)methyl)amine 
• 293328-23-1 2,2,5-trimethyl-3-(1'-p-aminomethylphenylethoxy)-4-phenyl-3-azahexane 

Relevant articles and documents

A modular approach toward functionalized three-dimensional macromolecules: From synthetic concepts to practical applications

A new strategy for the preparation of functional, multiarm star polymers via nitroxide-mediated "living" radical polymerization has been explored. The generality of this approach to the synthesis of three-dimensional macromolecular architectures allows for the construction of nanoscopically defined materials from a wide range of different homo, block, and random copolymers combining both apolar and polar vinylic repeat units. Functional groups can also be included along the backbone or as peripheral/chain end groups, thereby modulating the reactivity and polarity of defined portions of the stars. This modular approach to the synthesis of three-dimensional macromolecules permits the application of these tailored materials as multifunctional hosts for hydrogen bonding, nanoparticle formation, and as scaffolds for catalytic groups. Examples of applications of the functional stars in catalysis include their use in a Heck-type coupling as well as an enantioselective addition reaction.