Substance
ID:311078
Names and Identifiers
IUPAC Traditional name
4-(benzyloxy)-1H-indole
IUPAC name
4-(benzyloxy)-1H-indole
Synonyms
NSC 925394-Benzyloxyindole4-苄氧基吲哚
Properties
Safety Information
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
European Hazard Symbols
Irritant (Xi)Safety Statements
26-36
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
GHS Hazard statements
H315-H319-H335
German water hazard class
3
GHS Precautionary statements
P261-P305+P351+P338
GHS Signal Word
Warning
MSDS Link
Risk Statements
36/37/38
Product Information
Empirical Formula (Hill Notation)
C15H13NO
Purity
98%
Physical Property
Melting Point
57-61 °C(lit.)
Molecule Details
Packaging
1 g in glass bottle
Application
• Reactant for regioselective synthesis of oxopyrrolidine analogs via iodine-catalyzed Markovnikov addition1
• Reactant for preparation of indoles by Bartoli reductive cyclization as useful intermediates in medicinal chemistry research2
• Reactant for synthesis of carbon-11-labeled 4-aryl-4H-chromenes as new PET agents for imaging of apoptosis in cancer3
• Reactant for preparation of HCV inhibitors4
• Reactant for preparation of indol-3-yl tetramethylcyclopropyl ketones as CB2 cannabinoid receptor ligands5
• Reactant for preparation of 4-aryl-4H-chromenes as apoptosis inducers6
1 g in glass bottle
Application
• Reactant for regioselective synthesis of oxopyrrolidine analogs via iodine-catalyzed Markovnikov addition1
• Reactant for preparation of indoles by Bartoli reductive cyclization as useful intermediates in medicinal chemistry research2
• Reactant for synthesis of carbon-11-labeled 4-aryl-4H-chromenes as new PET agents for imaging of apoptosis in cancer3
• Reactant for preparation of HCV inhibitors4
• Reactant for preparation of indol-3-yl tetramethylcyclopropyl ketones as CB2 cannabinoid receptor ligands5
• Reactant for preparation of 4-aryl-4H-chromenes as apoptosis inducers6
Molecular Spectra
No Data Available
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References
No Data Available
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