1214741-20-4 - Names and Identifiers
Name | (3R,7aR)-3-(1,1-dimethylethyl)-7a-ethenyldihydro- 1H,3H-Pyrrolo[1,2-c]oxazole-1,5(6H)-dione
|
Synonyms | Methanone,[5-(bromomethyl)phenyl]phenyl- 3-Pyridinecarboxylicacid,2,10-dimethyl-,methylester (3R,7aR)-3-(tert-butyl)-7a-vinyldihydro-1H,3H-pyrrolo[1,2-c]oxazole-1,5(6H)-dione (3R,7aR)-3-tert-butyl-7a-ethenyl-6,7-dihydro-3H-pyrrolo[1,2-c][1,3]oxazole-1,5-dione (3R,7AR)-3-(1,1-DIMETHYLETHYL)-7A-ETHENYLDIHYDRO-1H,3H-PYRROLO[1,2-C]OXAZOLE-1,5(6H)-DIONE (3R,7Ar)-3-(1,1-dimethylethyl)-7A-ethenyldihydro-1H,3H-pyrrolo[1,2-C]oxazole-1,5(6H)-dione (3R,7aR)-3-(1,1-dimethylethyl)-7a-ethenyldihydro- 1H,3H-Pyrrolo[1,2-c]oxazole-1,5(6H)-dione 3-(1,1-diMethylethyl)-7a-ethenyldihydro-, (3R,7aR)-1H,3H-Pyrrolo[1,2-c]oxazole-1,5(6H)-dione 1H,3H-Pyrrolo[1,2-c]oxazole-1,5(6H)-dione, 3-(1,1-dimethylethyl)-7a-ethenyldihydro-, (3R,7aR)- 3-(1,1-diMethylethyl)-7a-ethenyldihydro-,(3R,7aR)-1H,3H-Pyrrolo[1,2-c]oxazole-1,5(6H)-dione1214741-20-4
|
CAS | 1214741-20-4
|
1214741-20-4 - Physico-chemical Properties
Molecular Formula | C12H17NO3
|
Molar Mass | 223.27 |
Density | 1.15±0.1 g/cm3(Predicted) |
Boling Point | 376.8±42.0 °C(Predicted) |
pKa | -2.14±0.60(Predicted) |
Storage Condition | 2-8°C |
1214741-20-4 - Introduction
3-(1,1-dimethylethyl)-7a-vinyldihydro-(3R,7aR)-1H, 3H-pyrrole [1,2-c] oxazole -1,5(6H)-dione, often abbreviated as EPD. The following is a description of the nature, use, formulation and safety information of EPD:
Nature:
EPD is a complex organic compound with solid form and is soluble in anhydrous organic solvents such as ethyl acetate and dichloromethane at room temperature. The molecular formula of EPD is C13H15NO3 and the molecular weight is 233.3g/mol.
Use:
EPD has certain application value in chemical research and pharmaceutical field. It can be used as an intermediate in organic synthesis for the synthesis of biologically active compounds and drugs. EPD can also be used to prepare novel materials and functional ligands.
Preparation Method:
There are many ways to prepare EPD. One common method is through the reaction of 4-(1,1-dimethylethyl) pyrrolo [1,2-c] oxazol-3-one (DMPT) and vinyl bromide (or vinyl chloride). In the specific operation, DMPT and vinyl alkyl halide are reacted under the catalysis of a base to finally obtain EPD.
Safety Information:
EPD is relatively stable under normal temperature and pressure, and is safer under proper use and storage. However, as a chemical, it is still dangerous. Exposure to EPD may cause eye and skin irritation. Avoid swallowing and keep away from sources of ignition. Wear appropriate personal protective equipment such as gloves and goggles when in use. When using EPDs in laboratory and industrial environments, the relevant safety practices should be observed.
Last Update:2024-04-09 20:45:29