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M14900

5-Methoxyindole

Name: 5-Methoxyindole
Brand: ALDRICH

99%

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About This Item

Empirical Formula (Hill Notation):

C₉H₉NO

CAS Number:

1006-94-6

Molecular Weight:

147.17

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24896650

EC Number:

213-745-3

Beilstein/REAXYS Number:

116722

MDL number:

MFCD00005674

Assay:

99%

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Properties

Quality Level

100

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

Description

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Optimization of the interligand Overhauser effect for fragment linking: application to inhibitor discovery against Mycobacterium tuberculosis pantothenate synthetase.

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

Simultaneous liquid chromatographic measurement of melatonin and related indoles through post-column electrochemical demethylation and fluorescence derivatization.

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

Rotationally resolved electronic spectroscopy of 5-methoxyindole.

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

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Global Trade Item Number

SKU	GTIN
M14900-1G	04061834040705
M14900-5G	04061834040712