Methyl 6-methoxy-2-indolecarboxylate

• Catalog No.: 365572
• CAS Number: 98081-83-5
• M. F.: C11H11NO3
• M. W.: 205.20994
• Purity: 99%

SYNONYMS

• Title: 6-甲氧基-2-吲哚羧酸甲酯
• IUPAC name: methyl 6-methoxy-1H-indole-2-carboxylate
• IUPAC Traditional name: methyl 6-methoxy-1H-indole-2-carboxylate
• Synonyms: 6-Methoxyindole-2-carboxylic acid methyl ester; 2-Methoxycarbonyl-6-methoxyindole

DATABASE IDS

• CAS Number: 98081-83-5
• MDL Number: MFCD00134301
• PubChem SID: 24862540

PROPERTIES

• Empirical Formula (Hill Notation): C11H11NO3
• Purity: 99%
• Melting Point: 117-119 °C(lit.)
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1 g in glass bottle
Application
Reactant for preparation of:
• Benzoxazole containing indole analogs as peroxisome proliferator-activated receptor-γ/δ dual agonists1
• Potent antiproliferative agent against human leukemia K562 cells2
• Indole-indolone scaffold via [3+2] annulation of arynes3
• Latonduine derivatives via intramolecular Heck reaction as possible anticancer agents4
• Arylthioindoles as potent inhibitors of tubulin polymerization5
• Heterocycle-fused derivatives of 1-oxo-1,2,3,4-tetrahydropyrazine via Ugi condensation6
• Indole fatty alcohols (IFAs) as promoters of differentiation of neural stem cell derived neurospheres into neurons. Potential application for treatment of neurodegenerative diseases7
• Light-dependent tumor necrosis factor-α antagonists8
• 2-substituted indole melatonin receptor ligands9

Description (简体中文)

包装
1 g in glass bottle
Application
Reactant for preparation of:
• Benzoxazole containing indole analogs as peroxisome proliferator-activated receptor-γ/δ dual agonists1
• Potent antiproliferative agent against human leukemia K562 cells2
• Indole-indolone scaffold via [3+2] annulation of arynes3
• Latonduine derivatives via intramolecular Heck reaction as possible anticancer agents4
• Arylthioindoles as potent inhibitors of tubulin polymerization5
• Heterocycle-fused derivatives of 1-oxo-1,2,3,4-tetrahydropyrazine via Ugi condensation6
• Indole fatty alcohols (IFAs) as promoters of differentiation of neural stem cell derived neurospheres into neurons. Potential application for treatment of neurodegenerative diseases7
• Light-dependent tumor necrosis factor-α antagonists8
• 2-substituted indole melatonin receptor ligands9