157427-91-3

Basic information

• Product Name: [4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-carbamic acid tert-butyl ester
• Synonyms: [4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-carbamic acid tert-butyl ester
• CAS NO: 157427-91-3
• Molecular Weight: 323.508
• Mol File: 157427-91-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-carbamic acid tert-butyl ester(157427-91-3)
• EPA Substance Registry System: [4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-carbamic acid tert-butyl ester(157427-91-3)

Safety Data

• Hazardous Substances Data: 157427-91-3(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 111359-74-1 4-[(tert-butyldimethylsilyl)oxy]aniline 
• 54840-15-2 4-N-tert-butoxycarbonylaminophenol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 123-30-8 4-amino-phenol 

Downstream Products

• 1259391-85-9 C₂₃H₃₉NO₄Si 
• 1259391-87-1 C₂₁H₃₂F₃NO₄Si 
• 1259391-91-7 C₂₆H₃₆FNO₄Si 
• 1259391-83-7 C₂₄H₃₃NO₄Si 
• 1259391-81-5 C₁₉H₃₁NO₄Si 
• 1259391-89-3 C₂₅H₃₅NO₅Si 
• 1259391-79-1 C₂₆H₃₇NO₄Si 
• 54840-15-2 4-N-tert-butoxycarbonylaminophenol 
• 916263-10-0 (R)-{2-[2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-yl)-acetyl]-4-hydroxy-phenyl}-carbamic acid tert-butyl ester 
• 229032-21-7 (S)-{4-(tert-butyl-dimethyl-silanyloxy)-2-[2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-yl)-acetyl]-phenyl}-carbamic acid tert-butyl ester 

Relevant articles and documents

Catalytic Dealkylative Synthesis of Cyclic Carbamates and Ureas via Hydrogen Atom Transfer and Radical-Polar Crossover

Guided by the transition-metal hydrogen atom transfer and radical-polar crossover concepts, we developed a functional-group-tolerant and scalable method for the synthesis of cyclic carbamates and ureas, which are found in the structures of bioactive compo

Synthetic Studies on Dynemicin A. New Quinoline Synthesis for C, D and E Rings

The important intermediates for the syntheses of dynemicin A model compounds were prepared by coupling between aryltin compounds and α-bromoenone derivatives in the presence of palladium catalyst.The products were transformed under acidic conditions to su