- 4-Benzyloxyindole
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- $122.00 / 1KG
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2024-01-11
- CAS:20289-26-3
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
- 4-Benzyloxyindole
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- $20.00 / 1kg
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2023-09-27
- CAS:20289-26-3
- Min. Order: 1kg
- Purity: 0.99
- Supply Ability: 20 tons
- 4-Benzyloxyindole
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- $0.00 / 1KG
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2023-09-06
- CAS:20289-26-3
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 500000kg
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| | 4-Benzyloxyindole Basic information |
| | 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) | | form | Solid | | pka | 17.17±0.30(Predicted) | | color | Beige to Brown | | BRN | 183150 | | CAS DataBase Reference | 20289-26-3(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37/39 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29339990 |
| | 4-Benzyloxyindole Usage And Synthesis |
| 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.
- Reactant for regioselective synthesis of oxopyrrolidine analogs via iodine-catalyzed Markovnikov addition
- Reactant for preparation of indoles by Bartoli reductive cyclization as useful intermediates in medicinal chemistry research
- Reactant for synthesis of carbon-11-labeled 4-aryl-4H-chromenes as new PET agents for imaging of apoptosis in cancer
- Reactant for preparation of HCV inhibitors.
- Reactant for preparation of indol-3-yl tetramethylcyclopropyl ketones as CB2 cannabinoid receptor ligands
- 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 |
| | 4-Benzyloxyindole Preparation Products And Raw materials |
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