Substance
ID:339277
Names and Identifiers
IUPAC Traditional name
1-methylindole-3-carbaldehyde
IUPAC name
1-methyl-1H-indole-3-carbaldehyde
Synonyms
NSC 830421-Methylindole-3-carboxaldehyde3-Formyl-1-methylindole1-甲基吲哚-3-甲醛
Properties
Safety Information
GHS Precautionary statements
P261-P305+P351+P338
German water hazard class
3
GHS Hazard statements
H315-H319-H335
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
MSDS Link
GHS Signal Word
Warning
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Risk Statements
36/37/38
Safety Statements
26-37/39
European Hazard Symbols
Irritant (Xi)Product Information
Empirical Formula (Hill Notation)
C10H9NO
Purity
97%
Physical Property
Melting Point
70-72 °C(lit.)
Molecule Details
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
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
Molecular Spectra
No Data Available
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References
No Data Available
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