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H31859

5-Hydroxyindole

Name: 5-Hydroxyindole
Brand: ALDRICH

97%

Synonym(s):

5-Indolol, 5-Hydroxyindole, NSC 87503

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About This Item

Empirical Formula (Hill Notation):

C₈H₇NO

CAS Number:

1953-54-4

Molecular Weight:

133.15

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24895561

EC Number:

217-782-6

Beilstein/REAXYS Number:

112349

MDL number:

MFCD00005677

Assay:

97%

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Properties

Quality Level

100

assay

97%

mp

106-108 °C (lit.)

SMILES string

Oc1ccc2[nH]ccc2c1

InChI

1S/C8H7NO/c10-7-1-2-8-6(5-7)3-4-9-8/h1-5,9-10H

InChI key

LMIQERWZRIFWNZ-UHFFFAOYSA-N

Description

Application

Reactant for preparation of (oxoimidazolidinyl/oxopyrimidinyl)benzenesulfonates as antitumor agents and tubulin inhibitors
Reactant for preparation of anthranilic acids
Reactant for preparation of indole compounds as dopamine D2 receptor antagonists
Reactant for preparation of naphthalimide- or carbazole-containing human β-adrenoceptor ligands
Reactant for preparation of melanins as nature-inspired radioprotectors
Reactant for preparation of 5-vinyl-3-pyridinecarbonitriles as PKCθ inhibitors

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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Ribosomal synthesis of cyclic peptides with a fluorogenic oxidative coupling reaction.

Yusuke Yamagishi et al.

Chembiochem : a European journal of chemical biology, 10(9), 1469-1472 (2009-05-28)

Electronic structure of 5-hydroxyindole: from gas phase to explicit solvation.

David Robinson et al.

The journal of physical chemistry. B, 113(8), 2535-2541 (2009-02-07)

We have investigated the absorption and emission spectrum of 5-hydroxyindole in the gas phase and in various solvents. 5-Hydroxyindole is the fluorophore of the non-natural amino acid 5-hydroxytryptophan, which has attracted recent interest as a novel intrinsic probe for protein

Simultaneous analysis of 29 synthetic cannabinoids and metabolites, amphetamines, and cannabinoids in human whole blood by liquid chromatography-tandem mass spectrometry - A New Zealand perspective of use in 2018.

Rui Shen Ong et al.

Drug testing and analysis, 12(2), 195-214 (2019-10-09)

We describe the validation of a method for the simultaneous analysis of 29 synthetic cannabinoids (SCs) and metabolites, 4 amphetamines, and 2 cannabinoids in human whole blood. This method enables one analysis to cover what previously required multiple analyses for

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Global Trade Item Number

SKU	GTIN
H31859-1G	04061833792858