121025-48-7

Basic information

• Product Name: C₁₉H₂₅NOSi
• CAS NO: 121025-48-7
• Molecular Weight: 311.499
• Mol File: 121025-48-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₉H₂₅NOSi(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₉H₂₅NOSi(121025-48-7)
• EPA Substance Registry System: C₁₉H₂₅NOSi(121025-48-7)

Safety Data

• Hazardous Substances Data: 121025-48-7(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 69589-21-5 O-tert-butyldimethylsilyl-2-aminophenol 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 1450761-17-7 (S,E)-2-(4-benzyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)-1-(4-bromophenyl)ethanone oxime 
• 1450761-11-1 (S)-1-(4-benzyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)pentan-2-one 
• 1450761-10-0 (S)-1-(4-benzyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)butan-2-one 
• 1450761-09-7 (S)-1-(4-benzyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)propan-2-one 
• 1450761-08-6 C₂₇H₂₃NO₂ 
• 1450761-07-5 (S)-2-(4-benzyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)-1-(4-nitrophenyl)ethanone 
• 1450761-06-4 (S)-2-(4-benzyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)-1-(4-chlorophenyl)ethanone 
• 1450761-05-3 (S)-2-(4-benzyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)-1-(4-bromophenyl)ethanone 
• 1450761-04-2 (S)-2-(4-benzyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)-1-(2-bromophenyl)ethanone 
• 1450761-03-1 (S)-2-(4-benzyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)-1-(4-methoxyphenyl)ethanone 
• 1450761-02-0 (S)-2-(4-benzyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)-1-(p-tolyl)ethanone 
• 1450761-14-4 2-(allyl(benzyl)amino)phenol 
• 881653-57-2 N-benzyl-2-((tert-butyldimethylsilyl)oxy)aniline 

Relevant articles and documents

Enantioselective synthesis of benzofurans and benzoxazines via an olefin cross-metathesis-intramolecular oxo-Michael reaction

Chiral phosphoric acid and Hoveyda-Grubbs II were found to catalyze an olefin cross-metathesis-intramolecular oxo-Michael cascade reaction of the ortho-allylphenols and enones to provide a variety of benzofuran and benzoxazine derivatives in moderate to good yields and enantioselectivity.