6-Hydroxyindole

6-Hydroxyindole
  • CAS No.:2380-86-1
Other grades of this product :
6-Hydroxyindole Basic information
Product Name:6-Hydroxyindole
Synonyms:1H-INDOL-6-OL;6-INDOLOL;6-HYDROXYINDOLE;INDOLOL;5.7-dichloroindole 2380-86-1;6-Hydroyindole;6-Hydroxy-1H-indole 95%;6-Hydroxyindole in stock Factory
CAS:2380-86-1
MF:C8H7NO
MW:133.15
EINECS:417-020-4
Product Categories:Heterocycle-Indole series;Indole;blocks;IndolesOxindoles;Indoles and derivatives;Heterocycles series;Indoline & Oxindole;Indoles
Mol File:2380-86-1.mol
6-Hydroxyindole Chemical Properties
Melting point 125-128 °C
Boiling point 343.2±15.0 °C(Predicted)
density 1.327±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
pka10.07±0.40(Predicted)
form Shiny Crystalline Powder
color White to off-white
InChIKeyXAWPKHNOFIWWNZ-UHFFFAOYSA-N
CAS DataBase Reference2380-86-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,N,Xn
Risk Statements 36/37/38-51/53-43-41-22
Safety Statements 37/39-26-61-24-2
RIDADR UN 3077
WGK Germany 3
Hazard Note Irritant
HazardClass IRRITANT, KEEP COLD
HazardClass 9
PackingGroup 
HS Code 29339900
MSDS Information
ProviderLanguage
ACROS English
6-Hydroxyindole Usage And Synthesis
Chemical PropertiesWhite to off-white shiny crystalline powder
Uses
  • Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators
  • Reactant for asymmetrical synthesis of notoamide J as a potential biosynthetic precursor of prenylated indole alkaloids
  • Reactant for preparation of (quinolinyloxymethyl)isoxazolecarboxylate esters antituberculosis agents
  • Reactant for preparation of indolyl(propanolamine) derivatives as HIV inhibitors
  • Reactant for preparation of indoleoxyacetic acid derivatives as peroxisome proliferator-activated receptor agonists
  • Reactant for preparation of 1-aroylindole 3-aroylindoles combretastatin A-4 analogs as antitumor agents and tubulin polymerization inhibitors
Synthesis Reference(s)Journal of Medicinal Chemistry, 35, p. 2419, 1992 DOI: 10.1021/jm00091a010

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