6-Methylindole

• Catalog No.: 67604
• CAS Number: 3420-02-8
• M. F.: C9H9N
• M. W.: 131.17446
• Purity: ≥98.0% (GC)

SYNONYMS

• Title: 6-甲基吲哚
• IUPAC name: 6-methyl-1H-indole
• IUPAC Traditional name: 6-methyl-1H-indole

DATABASE IDS

• CAS Number: 3420-02-8
• MDL Number: MFCD00005682
• Beilstein Number: 109708

PROPERTIES

• Empirical Formula (Hill Notation): C9H9N
• Grade: purum
• Purity: ≥98.0% (GC)
• Boiling Point: 112 °C/5 mmHg(lit.)
• Density: 1.059 g/mL at 25 °C(lit.)
• Flash Point: 110 °C
• Flash Point: 230 °F
• Refractive Index: n20/D 1.607(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (English)

Application

• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Reactant for preparation of indole linked triazole derivatives as antifungal agents2
• Reactant for preparation of N-β-D-xylosyl-indole derivatives as SGLT2 inhibitors for management of hyperglycemia in diabetes3
• Reactant for preparation of aminoguanidine derivatives of arylsulfonylacylindoles as antifungal agents4
• Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors5
• Reactant for preparation of arylsulfonylacetylindoles as anti-HIV-1 agents6

Description (简体中文)

Application

• Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1
• Reactant for preparation of indole linked triazole derivatives as antifungal agents2
• Reactant for preparation of N-β-D-xylosyl-indole derivatives as SGLT2 inhibitors for management of hyperglycemia in diabetes3
• Reactant for preparation of aminoguanidine derivatives of arylsulfonylacylindoles as antifungal agents4
• Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors5
• Reactant for preparation of arylsulfonylacetylindoles as anti-HIV-1 agents6