6-Methoxyindole
6-Methoxyindole Basic information
- Product Name:
- 6-Methoxyindole
- Synonyms:
-
- 6-Methoxyindole, 98% 500MG
- 6-methoxy-1H-indole(SALTDATA: FREE)
- 6-Methoxy-1H-indole 98%
- 6-(Methyloxy)-1H-indole
- NSC 92517
- Indole, 6-methoxy-
- 1H-Indole, 6-methoxy-
- 1H-INDOL-6-YL METHYL ETHER
- CAS:
- 3189-13-7
- MF:
- C9H9NO
- MW:
- 147.17
- EINECS:
- 221-689-6
- Product Categories:
-
- Indole
- Pyrroles & Indoles
- Indole and Indoline
- Simple Indoles
- Building Blocks
- Heterocyclic Building Blocks
- blocks
- IndolesOxindoles
- Indole/indoline/oxindole
- pharmacetical
- Pyrroles & Indoles
- Indoles
- Indole Series
- Indole Derivatives
- Heterocycle-Indole series
- bc0001
- Mol File:
- 3189-13-7.mol
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6-Methoxyindole Chemical Properties
- Melting point:
- 90-92 °C (lit.)
- Boiling point:
- 105°C 0,2mm
- Density
- 1.169±0.06 g/cm3(Predicted)
- Flash point:
- 105°C/0.2mm
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- solubility
- Methanol (Slightly)
- pka
- 17.22±0.30(Predicted)
- form
- Shiny Crystals
- color
- White
- Sensitive
- Light Sensitive
- BRN
- 116483
- InChIKey
- QJRWYBIKLXNYLF-UHFFFAOYSA-N
- CAS DataBase Reference
- 3189-13-7(CAS DataBase Reference)
- NIST Chemistry Reference
- Indole, 6-methoxy-(3189-13-7)
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MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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6-Methoxyindole Usage And Synthesis
Chemical Properties
white shiny crystals
Uses
6-Methoxyindole was used to study the fluorescence of protonated excited-state forms of serotonin and other related compounds in acid. It was used in the preparation of:
- tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles, potential anticancer immunomodulator
- indolylindazoles and indolylpyrazolopyridines, interleukin-2 inducible T cell kinase inhibitors
- diindolyloxyindoles, anticancer agents
- benzoylpiperazinyl-indolyl ethane dione derivatives, HIV-1 inhibitors
- 3-aroylindoles as anticancer agents
- indolyl and isoquinolinyl anthranilates, PPARδ partial agonists
- heteroaryl ketones, VEGFR-2 inhibitors
Synthesis Reference(s)
Synthesis, p. 735, 1986 DOI: 10.1055/s-1986-31759
Biochem/physiol Actions
6-Methoxyindole inhibits the chlorinating activity of myeloperoxidase and inhibits the generation of hypochlorous acid released by activated leukocytes.
6-Methoxyindole Preparation Products And Raw materials
Preparation Products
BANISTERINE MONOHYDRATE(S)-2-AMINO-3-(6-METHOXY-1H-INDOL-3-YL)-PROPIONIC ACID6-Methoxy-1H-indole-3-carbaldehyde
Raw materials
6-MethoxyindoleSupplier
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