474924-65-7

Basic information

• Product Name: allyl-(4-methoxy-phenyl)-carbamic acid tert-butyl ester
• Synonyms: allyl-(4-methoxy-phenyl)-carbamic acid tert-butyl ester
• CAS NO: 474924-65-7
• Molecular Weight: 263.337
• Mol File: 474924-65-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: allyl-(4-methoxy-phenyl)-carbamic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: allyl-(4-methoxy-phenyl)-carbamic acid tert-butyl ester(474924-65-7)
• EPA Substance Registry System: allyl-(4-methoxy-phenyl)-carbamic acid tert-butyl ester(474924-65-7)

Safety Data

• Hazardous Substances Data: 474924-65-7(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 24424-99-5 di-tert-butyl dicarbonate 
• 18437-68-8 tert-butyl N-(4-methoxyphenyl)carbamate 
• 106-95-6 allyl bromide 

Downstream Products

• 1380209-15-3 2-allyl-1-azido-4-methoxybenzene 
• 68267-68-5 2-allyl-4-methoxyaniline 
• 1374693-94-3 C₂₈H₃₁NO₇S 
• 1361121-57-4 C₂₀H₂₁NO₃S 
• 66236-30-4 C₁₇H₁₉NO₃S 
• 1361121-48-3 (E)-4-methoxy-2-(prop-1-en-1-yl)aniline 
• 71954-46-6 N-allyl-4-methoxyaniline 
• 528869-41-2 (Z)-(4-hydroxy-6-phenyl-hex-1-enyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester 

Relevant articles and documents

A new entry to the phenanthridine ring system

A new synthesis of phenanthridine derivatives having three-point diversity has been developed based on the sequential application of three-atom economic processes viz. aza-Claisen rearrangement, ring-closing enyne metathesis and Diels-Alder reaction as key steps. An unexpected isomerisation was observed during aza-Claisen rearrangement of N-allylanilines which may open up new opportunities in heterocyclic synthesis.

Pd(II)-catalyzed enantioselective oxidative tandem cyclization reactions. Synthesis of indolines through C-N and C-C bond formation

We have developed an efficient Pd(II)-catalyzed enantioselective oxidative tandem cyclization strategy using molecular oxygen as a green oxidant for the double 5-exo-trig cyclizations of N-(2-allylaryl) amides to afford a variety of indolines in good yiel