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1-Methylindole-3-carboxaldehyde

ALDRICH/357987 - 97%

Synonym: 3-Formyl-1-methylindole; NSC 83042

CAS Number: 19012-03-4
Empirical Formula (Hill Notation): C10H9NO
Molecular Weight: 159.18
EC Number: 242-750-3
MDL Number: MFCD00014570
Linear Formula: C10H9NO
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-357987-5G 5 g
$74.50
1/EA
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assay 97%
InChI 1S/C10H9NO/c1-11-6-8(7-12)9-4-2-3-5-10(9)11/h2-7H,1H3
InChI key KXYBYRKRRGSZCX-UHFFFAOYSA-N
mp 70-72 °C (lit.)
SMILES string Cn1cc(C=O)c2ccccc12
Application: • Reactant for preparation of nitroolefins and β-nitroalcohols via microwave- or ultrasound-assisted Henry reactions
• Reactant for synthesis of quinolinones via three-component Ugi reaction
• Reactant for synthesis of α-ketoamides as inhibitors of Dengue virus protease with antiviral activity in cell-culture
• Reactant for preparation of thiazolopyrimidinones as inhibitors of Bcl-2 proteins
• Reactant for preparation of vinylindoles via Peterson olefination or olefination with Nysted reagent
• Reactant for preparation of indolyl alkenes from microwave-enhanced Knoevenagel condensation as antibacterial agents
Application: 1-Methylindole-3-carboxaldehyde may be used in the synthesis of (Z)-3-(1-methyl-1H-indol-3-yl)-2-(thiophen-3-yl)acrylonitrile, via base-catalyzed condensation with thiophene-3-acetonitrile. It was also used in the preparation of monomer, required for the synthesis of poly(3-vinyl-1-methylindole).
General description: 1-Methylindole-3-carboxaldehyde is a heterocyclic indole aldehyde. 1-Methylindole-3-carboxaldehyde on condensation with 2-hydroxybenzohydrazide yields Schiff base.
Packaging: 5, 25 g in glass bottle
Purity 97%
mp 70-72 °C (lit.)
UNSPSC 12352100

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