1-Methylindole-3-carboxaldehyde

• Catalog No.: 357987
• CAS Number: 19012-03-4
• M. F.: C10H9NO
• M. W.: 159.18456
• Purity: 97%

SYNONYMS

• Title: 1-甲基吲哚-3-甲醛
• IUPAC name: 1-methyl-1H-indole-3-carbaldehyde
• IUPAC Traditional name: 1-methylindole-3-carbaldehyde
• Synonyms: 3-Formyl-1-methylindole; NSC 83042

DATABASE IDS

• PubChem SID: 24861954
• CAS Number: 19012-03-4
• MDL Number: MFCD00014570
• EC Number: 242-750-3

PROPERTIES

• Empirical Formula (Hill Notation): C10H9NO
• Purity: 97%
• Melting Point: 70-72 °C(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-37/39
• German water hazard class: 3

DETAILS

Description (English)

Packaging
5, 25 g in glass bottle
Application

• Reactant for preparation of nitroolefins and β-nitroalcohols via microwave- or ultrasound-assisted Henry reactions1
• Reactant for synthesis of quinolinones via three-component Ugi reaction2
• Reactant for synthesis of α-ketoamides as inhibitors of Dengue virus protease with antiviral activity in cell-culture3
• Reactant for preparation of thiazolopyrimidinones as inhibitors of Bcl-2 proteins4
• Reactant for preparation of vinylindoles via Peterson olefination or olefination with Nysted reagent5
• Reactant for preparation of indolyl alkenes from microwave-enhanced Knoevenagel condensation as antibacterial agents6

Description (简体中文)

包装
5, 25 g in glass bottle
Application

• Reactant for preparation of nitroolefins and β-nitroalcohols via microwave- or ultrasound-assisted Henry reactions1
• Reactant for synthesis of quinolinones via three-component Ugi reaction2
• Reactant for synthesis of α-ketoamides as inhibitors of Dengue virus protease with antiviral activity in cell-culture3
• Reactant for preparation of thiazolopyrimidinones as inhibitors of Bcl-2 proteins4
• Reactant for preparation of vinylindoles via Peterson olefination or olefination with Nysted reagent5
• Reactant for preparation of indolyl alkenes from microwave-enhanced Knoevenagel condensation as antibacterial agents6