6-BenzyloxyindoleCAS# 15903-94-3 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 15903-94-3 | SDF | Download SDF |
| PubChem ID | 260804 | Appearance | Powder |
| Formula | C15H13NO | M.Wt | 223.3 |
| Type of Compound | N/A | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 6-phenylmethoxy-1H-indole | ||
| SMILES | C1=CC=C(C=C1)COC2=CC3=C(C=C2)C=CN3 | ||
| Standard InChIKey | FPMICYBCFBLGOZ-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C15H13NO/c1-2-4-12(5-3-1)11-17-14-7-6-13-8-9-16-15(13)10-14/h1-10,16H,11H2 | ||
| General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
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| About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
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| Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. | ||
6-Benzyloxyindole Dilution Calculator
6-Benzyloxyindole Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 4.4783 mL | 22.3914 mL | 44.7828 mL | 89.5656 mL | 111.957 mL |
| 5 mM | 0.8957 mL | 4.4783 mL | 8.9566 mL | 17.9131 mL | 22.3914 mL |
| 10 mM | 0.4478 mL | 2.2391 mL | 4.4783 mL | 8.9566 mL | 11.1957 mL |
| 50 mM | 0.0896 mL | 0.4478 mL | 0.8957 mL | 1.7913 mL | 2.2391 mL |
| 100 mM | 0.0448 mL | 0.2239 mL | 0.4478 mL | 0.8957 mL | 1.1196 mL |
| * Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations. | |||||
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Acid-Promoted Competing Pathways in the Oxidative Polymerization of 5,6-Dihydroxyindoles and Related Compounds: Straightforward Cyclotrimerization Routes to Diindolocarbazole Derivatives.[Pubmed:11672324]
J Org Chem. 1998 Oct 2;63(20):7002-7008.
Oxidation of 5,6-dihydroxyindole (1a) in acidic aqueous media led to isomeric hexahydroxydiindolocarbazoles, isolated as the acetyl derivatives 5a (29%) and 6a (19%). When the reaction is stopped in the very early stages, small amounts of the indolylindoline 17 and the open trimer 18 can be isolated. Similar oxidation of the N-methyl (1b) and O,O-dimethyl (1c) derivatives of 1a, as well as of 5-methoxyindole (9b), 6-hydroxyindole (14a), and 6-Benzyloxyindole (14b), afforded the corresponding diindolocarbazoles 5b and 6b, 5c and 6c, 10, 16, and the related tetramer 15 in up to 70% overall yield, whereas 5,6-diacetoxyindole (1d), 5-hydroxyindole (9a), and indole failed to give cyclotrimerization products. Formation of diindolocarbazoles could be explained by a mechanism in which the electron-donating substituents propitiate an array of acid-induced couplings and subsequent dehydrogenation steps driven by the energetically favorable closure of the fused aromatic framework.
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