5,6-Dimethoxyindole

5,6-Dimethoxyindole Structure
CAS No.
14430-23-0
Chemical Name:
5,6-Dimethoxyindole
Synonyms
5,6-DIMETHOXY-1H-INDOLE;AKOS JY2083477;5,6-DIMETHOXYINDOLE;5,6-Dimethoxyindole,99%;5,6-Dimethoxyindole 99%;1H-Indole, 5,6-dimethoxy-;5,6-Dimethoxy-1H-indole99%;5,6-Dimethoxy-1H-indole 99%
CBNumber:
CB1129065
Molecular Formula:
C10H11NO2
Molecular Weight:
177.2
MOL File:
14430-23-0.mol
MSDS File:
SDS
Modify Date:
2024/6/13 17:03:25

5,6-Dimethoxyindole Properties

Melting point 154-157 °C (lit.)
Boiling point 198°C 8mm
Density 1.182±0.06 g/cm3(Predicted)
Flash point 198°C/8mm
storage temp. Sealed in dry,Room Temperature
pka 16.93±0.30(Predicted)
form Powder
color Beige
Water Solubility Insoluble in water.
λmax 306nm(EtOH)(lit.)
BRN 5683
InChIKey QODBZRNBPUPLEZ-UHFFFAOYSA-N
CAS DataBase Reference 14430-23-0(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P271-P280
Hazard Codes  Xi
Safety Statements  22-24/25
WGK Germany  3
10
HazardClass  IRRITANT
HS Code  29339900
NFPA 704
1
2 0

5,6-Dimethoxyindole price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 246255 5,6-Dimethoxyindole 99% 14430-23-0 1G ₹17666.4 2022-06-14 Buy
TCI Chemicals (India) D5148 5,6-Dimethoxyindole min. 98.0 % 14430-23-0 200MG ₹2800 2022-05-26 Buy
TCI Chemicals (India) D5148 5,6-Dimethoxyindole min. 98.0 % 14430-23-0 1G ₹11800 2022-05-26 Buy
Product number Packaging Price Buy
246255 1G ₹17666.4 Buy
D5148 200MG ₹2800 Buy
D5148 1G ₹11800 Buy

5,6-Dimethoxyindole Chemical Properties,Uses,Production

Chemical Properties

Beige powder

Uses

5,6-Dimethoxyindole is an indole derivative as analgesic antiinflammatory. It was used in the synthesis of N-benzyl-N-cyclopropyl-5,6-dimethoxyindole-3-glyoxalamide.

Application

5,6-Dimethoxyindole was used in the synthesis of N-benzyl-N-cyclopropyl-5,6-dimethoxyindole-3-glyoxalamide.
Reactant in synthesis of indolylhydroxyoxindoles via enantioselective Friedel-Crafts reaction
Reactant in synthesis of benzyl trimethoxyindoles
Reactant for synthesis of benzoylpiperazinyl-indolyl ethane dione derivatives as HIV-1 inhibitors
Reactant for synthesis of 1-aroylindole 3-aroylindoles combretastatin A-4 analogs as antitumor agents and tubulin polymerization inhibitors
Reactant for preparation of tryptophanol derivatives via the Grignard reaction

Synthesis Reference(s)

Journal of the American Chemical Society, 75, p. 5887, 1953 DOI: 10.1021/ja01119a030
Synthesis of 5,6-Dimethoxyindoles and 5,6-Dimethoxyoxindoles. A New Synthesis of Indoles DOI: 10.1021/ja01619a049

5,6-Dimethoxyindole Preparation Products And Raw materials

Raw materials

Preparation Products

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5,6-Dimethoxyindole,99% 5,6-Dimethoxy-1H-indole 99% 5,6-Dimethoxy-1H-indole99% AKOS JY2083477 5,6-DIMETHOXYINDOLE 1H-Indole, 5,6-dimethoxy- 5,6-Dimethoxyindole 99% 5,6-DIMETHOXY-1H-INDOLE 14430-23-0 14330-23-0 Building Blocks Heterocyclic Building Blocks Indoles Amines Aromatics Heterocyclic Compounds Indole Derivatives Building Blocks Heterocyclic Building Blocks Indoles Indoles and derivatives Indoline & Oxindole