H31859
5-Hydroxyindole
97%
Sinónimos:
5-Indolol, 5-Hydroxyindole, NSC 87503
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Fórmula empírica (notación de Hill):
C8H7NO
Número CAS:
Peso molecular:
133.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-782-6
Beilstein/REAXYS Number:
112349
MDL number:
Assay:
97%
Servicio técnico
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Permítanos ayudarleQuality Level
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
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
Clase de almacenamiento
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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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
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)
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