365572

Methyl-6-methoxy-2-indolcarboxylat

99%

• Synonym(e): 2-Methoxycarbonyl-6-methoxyindole, 6-Methoxyindole-2-carboxylic acid methyl ester
• Empirische Formel (Hill-System): C₁₁H₁₁NO₃
• CAS-Nummer: 98081-83-5
• Molekulargewicht: 205.21
• MDL-Nummer: MFCD00134301
• UNSPSC-Code: 12352100
• PubChem Substanz-ID: 24862540
• NACRES: NA.22

Eigenschaften

• Assay: 99%
• mp (Schmelzpunkt): 117-119 °C (lit.)
• Funktionelle Gruppe: ester
• SMILES String: COC(=O)c1cc2ccc(OC)cc2[nH]1
• InChI: 1S/C11H11NO3/c1-14-8-4-3-7-5-10(11(13)15-2)12-9(7)6-8/h3-6,12H,1-2H3
• InChIKey: OPUUCOLVBDQWEY-UHFFFAOYSA-N

Beschreibung

Anwendung

Methyl 6-methoxy-2-indolecarboxylate is suitable for use in the production of dyes by Escherichia coli expressing naphthalene dioxygenase (NDO) and toluene dioxygenase (TDO). It is also suitable for use in the production of dyes by Escherichia coli expressing multicomponent phenol hydroxylase (mPH) from Pseudomonas sp. strains KL33 and KL28.

Reactant for preparation of:

• Benzoxazole containing indole analogs as peroxisome proliferator-activated receptor-γ/δ dual agonists
• Potent antiproliferative agent against human leukemia K562 cells
• Indole-indolone scaffold via [3+2] annulation of arynes
• Latonduine derivatives via intramolecular Heck reaction as possible anticancer agents
• Arylthioindoles as potent inhibitors of tubulin polymerization
• Heterocycle-fused derivatives of 1-oxo-1,2,3,4-tetrahydropyrazine via Ugi condensation
• Indole fatty alcohols (IFAs) as promoters of differentiation of neural stem cell derived neurospheres into neurons. Potential application for treatment of neurodegenerative diseases
• Light-dependent tumor necrosis factor-α antagonists
• 2-substituted indole melatonin receptor ligands

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable