5,6-Dimethoxyindole

• Catalog No.: 38767
• CAS Number: 14430-23-0
• M. F.: C10H11NO2
• M. W.: 177.19984
• Purity: ≥98.0% (HPLC)

SYNONYMS

• Title: 5,6-二甲氧基吲哚
• IUPAC name: 5,6-dimethoxy-1H-indole
• IUPAC Traditional name: 5,6-dimethoxy-1H-indole

DATABASE IDS

• MDL Number: MFCD00005675
• CAS Number: 14430-23-0
• Beilstein Number: 5683
• EC Number: 238-402-5

PROPERTIES

• Empirical Formula (Hill Notation): C10H11NO2
• Grade: purum
• Purity: ≥98.0% (HPLC)
• Melting Point: 154-157 °C(lit.)
• Melting Point: 154-157 °C
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• German water hazard class: 3

DETAILS

Description (English)

Application

• Reactant in synthesis of indolylhydroxyoxindoles via enantioselective Friedel-Crafts reaction1
• Reactant in synthesis of benzyl trimethoxyindoles2
• Reactant for synthesis of benzoylpiperazinyl-indolyl ethane dione derivatives as HIV-1 inhibitors3
• Reactant for synthesis of 1-aroylindole 3-aroylindoles combretastatin A-4 analogs as antitumor agents and tubulin polymerization inhibitors4
• Reactant for preparation of tryptophanol derivatives via the Grignard reaction5

Description (简体中文)

Application

• Reactant in synthesis of indolylhydroxyoxindoles via enantioselective Friedel-Crafts reaction1
• Reactant in synthesis of benzyl trimethoxyindoles2
• Reactant for synthesis of benzoylpiperazinyl-indolyl ethane dione derivatives as HIV-1 inhibitors3
• Reactant for synthesis of 1-aroylindole 3-aroylindoles combretastatin A-4 analogs as antitumor agents and tubulin polymerization inhibitors4
• Reactant for preparation of tryptophanol derivatives via the Grignard reaction5