(S)-4-Benzyl-2-oxazolidinoneCAS# 90719-32-7 |
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| Cas No. | 90719-32-7 | SDF | Download SDF |
| PubChem ID | 736225 | Appearance | Powder |
| Formula | C10H11NO2 | M.Wt | 177 |
| Type of Compound | N/A | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | (4S)-4-benzyl-1,3-oxazolidin-2-one | ||
| SMILES | C1C(NC(=O)O1)CC2=CC=CC=C2 | ||
| Standard InChIKey | OJOFMLDBXPDXLQ-VIFPVBQESA-N | ||
| Standard InChI | InChI=1S/C10H11NO2/c12-10-11-9(7-13-10)6-8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,11,12)/t9-/m0/s1 | ||
| 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. | ||
(S)-4-Benzyl-2-oxazolidinone Dilution Calculator
(S)-4-Benzyl-2-oxazolidinone Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 5.6497 mL | 28.2486 mL | 56.4972 mL | 112.9944 mL | 141.2429 mL |
| 5 mM | 1.1299 mL | 5.6497 mL | 11.2994 mL | 22.5989 mL | 28.2486 mL |
| 10 mM | 0.565 mL | 2.8249 mL | 5.6497 mL | 11.2994 mL | 14.1243 mL |
| 50 mM | 0.113 mL | 0.565 mL | 1.1299 mL | 2.2599 mL | 2.8249 mL |
| 100 mM | 0.0565 mL | 0.2825 mL | 0.565 mL | 1.1299 mL | 1.4124 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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Stereoselective total synthesis of (+)-licochalcone E.[Pubmed:21910047]
Arch Pharm Res. 2011 Aug;34(8):1269-76.
The synthesis of (+)-licochalcone E (1) was accomplished for the first time in 13 steps from aryl bromide (6) with 8% overall yield. Palladium-catalyzed Negishi-Reformatsky coupling reaction of compound 6 with ethyl 2-(tributylstannyl)acetate provided the aryl acetic ester (5), which was converted to aryl acetamide (4) via mixed anhydride formation. Chiral auxiliarymediated methylation of the (S)-4-Benzyl-2-oxazolidinone-derived aryl acetamide (4) provided the key asymmetric benzylic methyl group in compound 1.
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