6-Hydroxyindole

• Catalog No.: 18805
• CAS Number: 2380-86-1
• M. F.: C8H7NO
• M. W.: 133.14728
• Purity: ≥99.0% (GC)

SYNONYMS

• Title: 6-羟基吲哚
• IUPAC name: 1H-indol-6-ol
• IUPAC Traditional name: 1H-indol-6-ol
• Synonyms: 6-Indolol; 吲哚醇

DATABASE IDS

• CAS Number: 2380-86-1
• EC Number: 417-020-4
• MDL Number: MFCD00152101

PROPERTIES

• European Hazard Symbols: Harmful (Xn)
• European Hazard Symbols: Nature polluting (N)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Faceshields, Gloves
• GHS Precautionary statements: P273-P280-P305 + P351 + P338
• RID/ADR: UN 3077 9/PG 3
• Risk Statements: 22-41-43-51/53
• Safety Statements: 24-26-37/39-61
• Hazard Class: 9
• UN Number: 3077
• Packing Group: 3
• German water hazard class: 2
• GHS Signal Word: Danger
• GHS Hazard statements: H302-H317-H318-H411
• Empirical Formula (Hill Notation): C8H7NO
• Purity: ≥99.0% (GC)
• Melting Point: 125-128 °C

DETAILS

Description (English)

Packaging
1 g in glass bottle
Application

• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Reactant for asymmetrical synthesis of notoamide J as a potential biosynthetic precursor of prenylated indole alkaloids2
• Reactant for preparation of (quinolinyloxymethyl)isoxazolecarboxylate esters antituberculosis agents3
• Reactant for preparation of indolyl(propanolamine) derivatives as HIV inhibitors4
• Reactant for preparation of indoleoxyacetic acid derivatives as peroxisome proliferator-activated receptor agonists5
• Reactant for preparation of 1-aroylindole 3-aroylindoles combretastatin A-4 analogs as antitumor agents and tubulin polymerization inhibitors6

Description (简体中文)

包装
1 g in glass bottle
Application

• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Reactant for asymmetrical synthesis of notoamide J as a potential biosynthetic precursor of prenylated indole alkaloids2
• Reactant for preparation of (quinolinyloxymethyl)isoxazolecarboxylate esters antituberculosis agents3
• Reactant for preparation of indolyl(propanolamine) derivatives as HIV inhibitors4
• Reactant for preparation of indoleoxyacetic acid derivatives as peroxisome proliferator-activated receptor agonists5
• Reactant for preparation of 1-aroylindole 3-aroylindoles combretastatin A-4 analogs as antitumor agents and tubulin polymerization inhibitors6