69589-21-5

Basic information

• Product Name: O-tert-butyldimethylsilyl-2-aminophenol
• Synonyms: O-tert-butyldimethylsilyl-2-aminophenol
• CAS NO: 69589-21-5
• Molecular Weight: 223.39
• Mol File: 69589-21-5.mol
• Article Data: 20

Chemical Properties

• CAS DataBase Reference: O-tert-butyldimethylsilyl-2-aminophenol(CAS DataBase Reference)
• NIST Chemistry Reference: O-tert-butyldimethylsilyl-2-aminophenol(69589-21-5)
• EPA Substance Registry System: O-tert-butyldimethylsilyl-2-aminophenol(69589-21-5)

Safety Data

• Hazardous Substances Data: 69589-21-5(Hazardous Substances Data)

Upstream product

• 18052-27-2 tert-butyldimethyl(phenoxy)silane 
• 88-75-5 2-hydroxynitrobenzene 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 158813-51-5 tert-butyldimethyl(2-nitrophenoxy)silane 
• 95-55-6 2-amino-phenol 

Downstream Products

• 165405-44-7 2-(tert-butyldimethylsilanyloxy)phenyl isocyanate 
• 121025-48-7 C₁₉H₂₅NOSi 
• 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 

Relevant articles and documents

Switchable Oxidative Reactions of N-allyl-2-Aminophenols: Palladium-Catalyzed Alkoxyacyloxylation vs an Intramolecular Diels-Alder Reaction

The Pd(II)-catalyzed reaction of N-allyl-2-aminophenols in the presence of PhI(OCOR)2 as the oxidant resulted in an alkoxyacyloxylation process, with the formation of functionalized dihydro-1,4-benzoxazines. The reaction performed in the absence of pallad

Nickel-catalyzed reductive aryl thiocarbonylation of alkene via thioester group transfer strategy

Herein reported is a nickel-catalyzed reductive aryl thiocarbonylation of alkene via thioester group transfer strategy by using simple and readily available thioesters. In contrast to traditional activation of weaker C(acyl)-S bond, the C(acyl)-C bond of

Nickel-Catalyzed Domino Heck Cyclization/Suzuki Coupling for the Synthesis of 3,3-Disubstituted Oxindoles

The first nickel-catalyzed domino Heck cyclization/Suzuki coupling reaction for the synthesis of 3,3-disubstituted oxindoles bearing quaternary all-carbon centers is reported. A wide range of electrophiles, such as aryl iodides, bromides, triflates, and c