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4-Benzyloxyindole_Molecular_structure_CAS_20289-26-3)
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4-Benzyloxyindole

Catalog No. 246212 Name Sigma Aldrich
CAS Number 20289-26-3 Website http://www.sigmaaldrich.com
M. F. C15H13NO Telephone 1-800-521-8956
M. W. 223.26982 Fax
Purity 98% Email
Storage Chembase ID: 11796

SYNONYMS

Title
4-苄氧基吲哚
IUPAC name
4-(benzyloxy)-1H-indole
IUPAC Traditional name
4-(benzyloxy)-1H-indole
Synonyms
NSC 92539

DATABASE IDS

MDL Number MFCD00047200
PubChem SID 24854794
EC Number 243-690-0
CAS Number 20289-26-3

PROPERTIES

Empirical Formula (Hill Notation) C15H13NO
Purity 98%
Melting Point 57-61 °C(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
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
Description (简体中文)
包装
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

REFERENCES