246298
4-Methoxyindole
99%
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About This Item
Formule empirique (notation de Hill):
C9H9NO
Numéro CAS:
Poids moléculaire :
147.17
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Niveau de qualité
Pureté
99%
Forme
powder
Point d'ébullition
181-183 °C/24 mmHg (lit.)
Pf
69-70 °C (lit.)
Solubilité
ethanol: 50 mg/mL, clear, faintly yellow
Chaîne SMILES
COc1cccc2[nH]ccc12
InChI
1S/C9H9NO/c1-11-9-4-2-3-8-7(9)5-6-10-8/h2-6,10H,1H3
Clé InChI
LUNOXNMCFPFPMO-UHFFFAOYSA-N
Application
4-Methoxyindole was used for comparing the complexation reaction of β-cyclodextrin (β-CD) with pindolol using reversed-phase liquid chromatography.
Reactant for preparation of:
- GABA analogs
- Sodium-Dependent Glucose Co-transporter 2 (SGLT2) Inhibitors for the Management of Hyperglycemia in Diabetes
- Anticancer agents
- Integrase strand-transfer inhibitors (INSTIs)
- Inhibitor of Proliferation of Colon Cancer Cells
- Isomeridianin G as GSK-3ß inhibitors
- HIV-1 integrase inhibitors
- Inhibitors of mitogen activated protein kinase-activated protein kinase 2 (MK-2)
Mention d'avertissement
Warning
Mentions de danger
Conseils de prudence
Classification des risques
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organes cibles
Respiratory system
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
dust mask type N95 (US), Eyeshields, Gloves
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Les clients ont également consulté
Carmen Gazpio et al.
Journal of pharmaceutical and biomedical analysis, 37(3), 487-492 (2005-03-03)
The complexation with beta-cyclodextrin (beta-CD) has been investigated using reversed-phase liquid chromatography. The compounds tested have been pindolol and, for comparison purposes, indole and 4-methoxyindole. The retention behaviour has been analysed on a Kromasil 100 C18 column and the mobile
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Applied biochemistry and biotechnology, 181(4), 1590-1610 (2016-11-11)
The enantioselective epoxidation of styrene and related compounds by two-component styrene monooxygenases (SMOs) has targeted these enzymes for development as biocatalysts. In the present work, we prepare genetically engineered fusion proteins that join the C-terminus of the epoxidase (StyA) to
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