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4-Benzyloxyindole

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
MDL Number:
MFCD00047200
MOL File:
20289-26-3.mol
MSDS File:
SDS
Last updated:2024-12-25 18:09:02

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
InChI InChI=1S/C15H13NO/c1-2-5-12(6-3-1)11-17-15-8-4-7-14-13(15)9-10-16-14/h1-10,16H,11H2
InChIKey LJFVSIDBFJPKLD-UHFFFAOYSA-N
SMILES N1C2=C(C(OCC3=CC=CC=C3)=CC=C2)C=C1
CAS DataBase Reference 20289-26-3(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
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(33)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 246212 4-Benzyloxyindole 98% 20289-26-3 1g $30 2023-06-20 Buy
TCI Chemical B2811 4-Benzyloxyindole >98.0%(GC) 20289-26-3 1g $77 2024-03-01 Buy
TCI Chemical B2811 4-Benzyloxyindole >98.0%(GC) 20289-26-3 5g $234 2024-03-01 Buy
Alfa Aesar L17147 4-Benzyloxyindole, 99% 20289-26-3 1g $96.3 2021-12-16 Buy
Alfa Aesar L17147 4-Benzyloxyindole, 99% 20289-26-3 250mg $33.1 2021-12-16 Buy
Product number Packaging Price Buy
246212 1g $30 Buy
B2811 1g $77 Buy
B2811 5g $234 Buy
L17147 1g $96.3 Buy
L17147 250mg $33.1 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.

Uses

Indole 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

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

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 7, p. 34, 1990
The Journal of Organic Chemistry, 51, p. 4294, 1986 DOI: 10.1021/jo00372a037
Tetrahedron Letters, 24, p. 4561, 1983 DOI: 10.1016/S0040-4039(00)85955-9

Synthesis

To a stirred solution of 162.2 g (0.50 mol) of (E)-6-benzyloxy-2-nitro-β-pyrrolidinostyrene in 1 L of THF and 1 L of methanol at 30°C under nitrogen is added 10 mL of Raney nickel followed by 44 mL (0.75 mol) of 85% hydrazine hydrate. Vigorous gas evolution is observed. The red color turns dark brown within 10 minutes, and the reaction temperature rises to 46°C. An additional 44 mL of 85% hydrazine hydrate is added after 30 min and again 1 hr later. The temperature is maintained between 45 and 50°C with a water bath during the reaction and for 2 hr after the last addition. The mixture is cooled to room temperature, and the catalyst is removed by filtration through a bed of Celite. The catalyst is washed several times with methylene chloride. The filtrate is evaporated, and the residue is dried by evaporating with 500 mL of toluene. The reddish residue (118.5 g), dissolved in ca. 1 L of toluene-cyclohexane (1 : 1), is applied to a column of 500 g of silica gel (70–230-mesh, Merck) prepared in the same solvent. Elution with 6.0 L of toluene–cyclohexane (1 : 1) followed by 3 L of toluene–cyclohexane (1 : 2) affords 108.3 g of white solid, which is crystallized from 150 mL of toluene and 480 mL of cyclohexane. 107.3 g (96% yield) of 4-benzyloxyindole is obtained in three crops as white prisms, mp 60–62°C.

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View Lastest Price from 4-Benzyloxyindole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
4-Benzyloxyindole pictures 2025-01-23 4-Benzyloxyindole
20289-26-3
US $1.00 / g 1g 99% 100kg Dorne Chemical Technology co. LTD
4-Benzyloxyindole pictures 2025-01-20 4-Benzyloxyindole
20289-26-3
US $0.00 / KG 1KG 98%min 30tons/month WUHAN FORTUNA CHEMICAL CO., LTD
4-Benzyloxyindole pictures 2025-01-10 4-Benzyloxyindole
20289-26-3
US $0.00-0.00 / kg 1kg 99 1000 Wuhan Circle Star Chem-medical Technology Co.,Ltd
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  • 4-Benzyloxyindole
    20289-26-3
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  • Wuhan Circle Star Chem-medical Technology Co.,Ltd
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