6-Hydroxyindole

6-Hydroxyindole Structure
CAS No.
2380-86-1
Chemical Name:
6-Hydroxyindole
Synonyms
1H-INDOL-6-OL;INDOLOL;6-INDOLOL;6(1H)-indolol;6-Hydroyindole;6-HydroxyindoL;6-HYDROXYINDOLE;6-carboxylindoline;6-Hydroxy-1H-indole;6-Hydroxyindole,97%
CBNumber:
CB1116076
Molecular Formula:
C8H7NO
Molecular Weight:
133.15
MOL File:
2380-86-1.mol
MSDS File:
SDS
Modify Date:
2024/6/6 20:41:42

6-Hydroxyindole 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
solubility Chloroform (Slightly, Heated), Methanol (Slightly)
pka 10.07±0.40(Predicted)
form Shiny Crystalline Powder
color White to off-white
InChIKey XAWPKHNOFIWWNZ-UHFFFAOYSA-N
CAS DataBase Reference 2380-86-1(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS05,GHS07,GHS09
Signal word  Danger
Hazard statements  H302-H317-H318-H411
Precautionary statements  P273-P280-P305+P351+P338
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
NFPA 704
1
2 0

6-Hydroxyindole price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 18805 6-Hydroxyindole ≥99.0% (GC) 2380-86-1 1G ₹24507.8 2022-06-14 Buy
Product number Packaging Price Buy
18805 1G ₹24507.8 Buy

6-Hydroxyindole Chemical Properties,Uses,Production

Chemical Properties

White 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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6-Hydroxyindole Spectrum

6-INDOLOL 6-HYDROXYINDOLE INDOLOL 5.7-dichloroindole 2380-86-1 6-Hydroyindole Indolol,6-Hydroxyindole 6-Hydroxyindole ,98% 6-Hydroxyindole,97% 6-HydroxyindoleIndolol 6-Hydroxy-1H-indole 6(1H)-indolol 6-Hydroxyindole, 97% 5GR 6-carboxylindoline 6-monohydroxyindole 6-Hydroxyindole≥ 99.5% (HPLC) 6-Hydroxyindole >=99.0% (GC) 6-Hydroxy-1H-indole 95% 6-Hydroxyindole in stock Factory 6-Hydroxyindole, 98%, reagent grade 6-HydroxyindoL 1H-INDOL-6-OL Pindolol Impurity 10 2380-86-1 Indoles Heterocyclic Building Blocks Building Blocks Heterocycle-Indole series Indole blocks IndolesOxindoles Indoles and derivatives Heterocycles series Indoline & Oxindole Indoles