Ethyl 1,3-thiazolidine-4-carboxylate
ethyl thiazolidine-4-carboxylate
CAS: 51977-21-0
Molecular Formula: C6H11NO2S
Ethyl 1,3-thiazolidine-4-carboxylate - Names and Identifiers
| Name | ethyl thiazolidine-4-carboxylate |
| Synonyms | Einecs 257-567-4 ethyl thiazolidine-4-carboxylate Ethyl thiazolidine-4-carboxylate Ethyl 1,3-thiazolidine-4-carboxylate ethyl 1,3-thiazolidine-4-carboxylate 4-Thiazolidine carboxylic ethyl ester Thiazolidine-4-carboxylic acid ethyl ester |
| CAS | 51977-21-0 |
| EINECS | 257-567-4 |
| InChI | InChI=1/C6H11NO2S/c1-2-9-6(8)5-3-10-4-7-5/h5,7H,2-4H2,1H3 |
Ethyl 1,3-thiazolidine-4-carboxylate - Physico-chemical Properties
| Molecular Formula | C6H11NO2S |
| Molar Mass | 161.22 |
| Density | 1.165±0.06 g/cm3(Predicted) |
| Boling Point | 90-91 °C(Press: 3 Torr) |
| Flash Point | 107.6°C |
| Vapor Presure | 0.0174mmHg at 25°C |
| pKa | 6.90±0.40(Predicted) |
| Refractive Index | 1.503 |
Ethyl 1,3-thiazolidine-4-carboxylate - Introduction
Ethyl thiazolidine-4-carboxylate is an organic compound with the chemical formula C7H11NO2S. Its appearance is a colorless or light yellow liquid with a special smell.
ethyl thiazolidine-4-carboxylate is commonly used as an intermediate or reagent in organic synthesis. It can be used for the synthesis of various thiazole and thiazolidine compounds, with certain pharmacological activity. In addition, it can also be used to synthesize fragrance or fragrance precursors.
The preparation method of ethyl thiazolidine-4-carboxylate is relatively simple. One commonly used method is the reaction of ethyl acetate with 4-chloroacetic acid thiazolidine under base catalysis to give ethyl thiazolidine-4-carboxylate.
When using ethyl thiazolidine-4-carboxylate, you need to pay attention to its safety. It may be irritating to the eyes and skin, so avoid direct contact with the skin and eyes. At the same time, ethyl thiazolidine-4-carboxylate is a flammable liquid and should be kept away from open flames and high temperatures. It is recommended to wear appropriate personal protective equipment such as gloves and goggles when handling or using.
ethyl thiazolidine-4-carboxylate is commonly used as an intermediate or reagent in organic synthesis. It can be used for the synthesis of various thiazole and thiazolidine compounds, with certain pharmacological activity. In addition, it can also be used to synthesize fragrance or fragrance precursors.
The preparation method of ethyl thiazolidine-4-carboxylate is relatively simple. One commonly used method is the reaction of ethyl acetate with 4-chloroacetic acid thiazolidine under base catalysis to give ethyl thiazolidine-4-carboxylate.
When using ethyl thiazolidine-4-carboxylate, you need to pay attention to its safety. It may be irritating to the eyes and skin, so avoid direct contact with the skin and eyes. At the same time, ethyl thiazolidine-4-carboxylate is a flammable liquid and should be kept away from open flames and high temperatures. It is recommended to wear appropriate personal protective equipment such as gloves and goggles when handling or using.
Last Update：2024-04-10 22:29:15
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Ethyl 1,3-thiazolidine-4-carboxylate
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ST 91
519044-91-8
Benzamide, N,N-diethyl-3-[(4-fluorobenzoyl)amino]-
29484-23-9
Nitrate de zinc
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