4-Benzyloxyindole

• Catalog No.: 246212
• CAS Number: 20289-26-3
• M. F.: C15H13NO
• M. W.: 223.26982
• Purity: 98%

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 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: 26-36
• 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