Substance
ID:333557
Names and Identifiers
IUPAC name
2,5-dimethyl-1H-indole
IUPAC Traditional name
1H-indole, 2,5-dimethyl-
Synonyms
2,5-Dimethylindole2,5-二甲基吲哚
Properties
Safety Information
GHS Signal Word
Danger
Risk Statements
37/38-41
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
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
European Hazard Symbols
Irritant (Xi)GHS Hazard statements
H315-H318-H335
MSDS Link
GHS Precautionary statements
P261-P280-P305+P351+P338
German water hazard class
3
Safety Statements
26-39
Product Information
Empirical Formula (Hill Notation)
C10H11N
Purity
97%
Physical Property
Melting Point
112-113 °C(lit.)
Molecule Details
Packaging
1 g in glass bottle
Application
• Reactant in stereoselective preparation of substituted indoles via rhodium-catalyzed enantioselective coupling reaction of indoles with diazo compounds1
• Reactant in stereoselective synthesis of indolines via palladium-catalyzed asymmetric hydrogenation of unprotected indoles2
• Reactant in enantioselective synthesis of fluorene derivatives via Friedel-Crafts reactions3
• Reactant in preparation of bis-indolyldihydroxybenzoquinones by addition indoles to dichlorobenzoquinone promoted by Bronsted acid4
• Reactant in reaction with hydroxypyrazolines5
1 g in glass bottle
Application
• Reactant in stereoselective preparation of substituted indoles via rhodium-catalyzed enantioselective coupling reaction of indoles with diazo compounds1
• Reactant in stereoselective synthesis of indolines via palladium-catalyzed asymmetric hydrogenation of unprotected indoles2
• Reactant in enantioselective synthesis of fluorene derivatives via Friedel-Crafts reactions3
• Reactant in preparation of bis-indolyldihydroxybenzoquinones by addition indoles to dichlorobenzoquinone promoted by Bronsted acid4
• Reactant in reaction with hydroxypyrazolines5
Molecular Spectra
No Data Available
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References
No Data Available
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