All Photos(1)

M14900

Sigma-Aldrich

5-Methoxyindole

99%

Empirical Formula (Hill Notation):
C9H9NO
CAS Number:
Molecular Weight:
147.17
Beilstein:
116722
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

bp

176-178 °C/17 mmHg (lit.)

mp

52-55 °C (lit.)

SMILES string

COc1ccc2[nH]ccc2c1

InChI

1S/C9H9NO/c1-11-8-2-3-9-7(6-8)4-5-10-9/h2-6,10H,1H3

InChI key

DWAQDRSOVMLGRQ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificate of Analysis

Certificate of Origin

Christian Brand et al.
The Journal of chemical physics, 133(2), 024303-024303 (2010-07-17)
Rotationally resolved electronic spectra of the vibrationless origin and of eight vibronic bands of 5-methoxyindole (5MOI) have been measured and analyzed using an evolutionary strategy approach. The experimental results are compared to the results of ab initio calculations. All vibronic
Kenichiro Todoroki et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 22(2), 281-286 (2006-03-04)
In this paper we describe a highly sensitive and selective liquid chromatographic method for the determination of 5-methoxyindoles (5-methoxyindole-3-acetic acid, 5-methoxytryptamine, 5-methoxytryptophol, and melatonin) using a post-column technique involving electrolytic demethylation followed by fluorescence derivatization with benzylamine. We separated these
Pawel Sledz et al.
Journal of the American Chemical Society, 132(13), 4544-4545 (2010-03-18)
Fragment-based methods are a new and emerging approach for the discovery of protein binders that are potential new therapeutic agents. Several ways of utilizing structural information to guide the inhibitor assembly have been explored to date. One of the approaches
F Peter Guengerich et al.
Journal of medicinal chemistry, 47(12), 3236-3241 (2004-05-28)
Indigoids, a class of bis-indoles, represent a promising protein kinase inhibitor scaffold. Oxidation of indole by cytochrome P450 (P450) has been shown to generate species (indoxyl, isatin) that couple to yield indigo and indirubin. Escherichia coli-expressed human P450 2A6 mutants
Lisa Cooper et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 24(23), 6105-6114 (2018-02-03)
Optimisation, scope and mechanism of the platinum-catalysed addition of indoles to indolylallenes is reported here to give 2,3'-BIMs with a novel core structure very relevant for pharmaceutical industry. The reaction is modulated by the electronic properties of the substituents on

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service