4-Benzyloxyindole

4-Benzyloxyindole
  • CAS No.:20289-26-3
Other grades of this product :
4-Benzyloxyindole Basic information
Product Name:4-Benzyloxyindole
Synonyms:4-(phenylmethoxy)-1h-indole;4-BENZYLOXY-1H-INDOLE;4-BENZYLOXYINDOLE;4-BENZYLOXYLINDOLE;NSC 92539;4-BENZYLOXYINDOLE 98%;{[(1H-Indol-4-yl)oxy]methyl}benzene;4-(Benzyloxy)-1H-indole 98%
CAS:20289-26-3
MF:C15H13NO
MW:223.27
EINECS:243-690-0
Product Categories:Simple Indoles;Indole;Chiral Compound;Aromatics;Indole Derivatives;Pyrroles & Indoles;blocks;IndolesOxindoles;Indoles and derivatives;Aromatics Compounds;Indoles;Building Blocks;Heterocyclic Building Blocks;Heterocycle-Indole series;Pyrroles & Indoles;Indoline & Oxindole;Indole Series;bc0001
Mol File:20289-26-3.mol
4-Benzyloxyindole Chemical Properties
Melting point 57-61 °C (lit.)
Boiling point 364.56°C (rough estimate)
density 1.0707 (rough estimate)
refractive index 1.5500 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
pka17.17±0.30(Predicted)
form Solid
color Beige to Brown
BRN 183150
CAS DataBase Reference20289-26-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
WGK Germany 3
HazardClass IRRITANT
HS Code 29339990
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
4-Benzyloxyindole Usage And Synthesis
Chemical PropertiesOff-White Crystalline Solid with Few Darker (Brown) Particles
UsesIndole derivative as substrate-binding; N297Q and I300V mutants of cytochrome P 450 2A6 display expansion of substrate specificity of cytochrome P 450 2A6 to oxidize substituted indoles
Uses4-Benzyloxyindole was used in the synthesis of 4-alkyloxy-aminoalkyl indole derivatives.
Reactions4-Benzyloxyindole was used in the synthesis of 4-alkyloxy-aminoalkyl indole derivatives.
  1. Reactant for regioselective synthesis of oxopyrrolidine analogs via iodine-catalyzed Markovnikov addition
  2. Reactant for preparation of indoles by Bartoli reductive cyclization as useful intermediates in medicinal chemistry research
  3. Reactant for synthesis of carbon-11-labeled 4-aryl-4H-chromenes as new PET agents for imaging of apoptosis in cancer
  4. Reactant for preparation of HCV inhibitors.
  5. Reactant for preparation of indol-3-yl tetramethylcyclopropyl ketones as CB2 cannabinoid receptor ligands
  6. Reactant for preparation of 4-aryl-4H-chromenes as apoptosis inducers
Synthesis Reference(s)Organic Syntheses, Coll. Vol. 7, p. 34, 1990The Journal of Organic Chemistry, 51, p. 4294, 1986 DOI: 10.1021/jo00372a037Tetrahedron Letters, 24, p. 4561, 1983 DOI: 10.1016/S0040-4039(00)85955-9
4-Benzyloxyindole Preparation Products And Raw materials

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