847577-89-3

Basic information

• Product Name: 4-Quinolinol, 6-(phenylMethoxy)-
• Synonyms: 4-Quinolinol, 6-(phenylMethoxy)-;6-Benzyloxy-quinolin-4-ol
• CAS NO: 847577-89-3
• Molecular Formula: C₁₆H₁₃NO₂
• Molecular Weight: 251.27992
• Mol File: 847577-89-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-Quinolinol, 6-(phenylMethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Quinolinol, 6-(phenylMethoxy)-(847577-89-3)
• EPA Substance Registry System: 4-Quinolinol, 6-(phenylMethoxy)-(847577-89-3)

Safety Data

• Hazardous Substances Data: 847577-89-3(Hazardous Substances Data)

Upstream product

• 909345-56-8 C₂₀H₁₉NO₅ 
• 2033-24-1 cycl-isopropylidene malonate 
• 6373-46-2 p-benzyloxyaniline 
• 847577-88-2 5-{[(4-benzyloxy)phenylimino]methyl}-2,2-dimethyl-[1,3]-dioxane-4,6-dione 

Downstream Products

• 847577-90-6 6-benzyloxy-3-nitroquinolin-4-ol 
• 863786-01-0 6-benzyloxy-4-chloroquinoline 

Relevant articles and documents

Enantioselective synthesis of cyclic α-aminoboronates via copper-catalyzed dearomative borylation of 4-quinolinols

A highly enantioselective and regioselective dearomative borylation of 4-quinolinols was developed using a Cu(i)/(R,R)-Ph-BPE catalyst for efficient synthesis of unprecedented heterocyclic α-amino boronates, a new class of compounds potentially relevant to drug discovery, in generally excellent yields and enantioselectivities. The products were also useful intermediates for highly functionalized tetrahydroquinolines and cyclic α-aminoboronate derivatives.

ARYLOXY AND ARYLALKYLENEOXY SUBSTITUTED IMIDAZOQUINOLINES

Imidazoquinoline compounds with an aryloxy or arylalkyleneoxy or hydroxy substituent at the 6, 7, 8, or 9-position, pharmaceutical compositions containing the compounds, intermediates, and methods of use of these compounds as immunomodulators, for modulating cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases, are disclosed.