4-Benzyloxyindole

4-Benzyloxyindole Structure
CAS No.
20289-26-3
Chemical Name:
4-Benzyloxyindole
Synonyms
NSC 92539;4-BENZYLOXYINDOLE;4-BENZYLOXYLINDOLE;4-Benzyloxyindole>4-BENZYLOXYINDOLE 98%;4-BENZYLOXY-1H-INDOLE;4-Benzyloxyindole,99%;4-Benzyloxyindole ,98%;4-(phenylmethoxy)-1h-indole;4-(Benzyloxy)-1H-indole 98%
CBNumber:
CB4319405
Molecular Formula:
C15H13NO
Molecular Weight:
223.27
MOL File:
20289-26-3.mol
MSDS File:
SDS
Modify Date:
2024/7/29 20:37:10

4-Benzyloxyindole 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)
form Solid
pka 17.17±0.30(Predicted)
color Beige to Brown
BRN 183150
CAS DataBase Reference 20289-26-3(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  3
HazardClass  IRRITANT
HS Code  29339990
NFPA 704
1
2 0

4-Benzyloxyindole price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 246212 4-Benzyloxyindole 98% 20289-26-3 1G ₹11041.5 2022-06-14 Buy
TCI Chemicals (India) B2811 4-Benzyloxyindole min. 98.0 % 20289-26-3 1G ₹5900 2022-05-26 Buy
TCI Chemicals (India) B2811 4-Benzyloxyindole min. 98.0 % 20289-26-3 5G ₹11700 2022-05-26 Buy
Product number Packaging Price Buy
246212 1G ₹11041.5 Buy
B2811 1G ₹5900 Buy
B2811 5G ₹11700 Buy

4-Benzyloxyindole Chemical Properties,Uses,Production

Chemical Properties

Off-White Crystalline Solid with Few Darker (Brown) Particles

Uses

4-Benzyloxyindole was used in the synthesis of 4-alkyloxy-aminoalkyl indole derivatives.

Reactions

4-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

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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% 4-Benzyloxyindole ,98% 1H-Indole, 4-(phenylMethoxy)- 4-Benzyloxyindole,99% 4-Benzyloxyindole 20289-26-3 4-(Phenylmethoxy)-1H-indole 20289-26-3 4-Benzyloxyindole in stock Factory 4-Benzyloxyindole> 20289-26-3 20286-26-3 20289-29-3 Indoles Simple Indoles Building Blocks Heterocyclic Building Blocks Simple Indoles Indole Chiral Compound Aromatics Indole Derivatives Pyrroles & Indoles Building Blocks Heterocyclic Building Blocks Indoles Heterocycle-Indole series blocks IndolesOxindoles Indoles and derivatives Aromatics Compounds Pyrroles & Indoles Indoline & Oxindole Indole Series bc0001