ethyl (2S)-2,3-dihydro-1,4-benzodioxine-2-carboxylate
Ethyl (2S)-2,3-dihydro-1,4-benzodioxine-2-carboxylate
CAS: 882980-86-1
Molecular Formula: C11H12O4
ethyl (2S)-2,3-dihydro-1,4-benzodioxine-2-carboxylate - Names and Identifiers
| Name | Ethyl (2S)-2,3-dihydro-1,4-benzodioxine-2-carboxylate |
| Synonyms | Ethyl (2S)-2,3-dihydro-1,4-benzodioxine-2-carboxylate (S)-ethyl 2,3-dihydrobenzo[b][1,4]dioxine-2-carboxylate 1,4-Benzodioxin-2-carboxylic acid, 2,3-dihydro-, ethyl ester, (2S)- |
| CAS | 882980-86-1 |
| InChI | InChI=1S/C11H12O4/c1-2-13-11(12)10-7-14-8-5-3-4-6-9(8)15-10/h3-6,10H,2,7H2,1H3/t10-/m0/s1 |
ethyl (2S)-2,3-dihydro-1,4-benzodioxine-2-carboxylate - Physico-chemical Properties
| Molecular Formula | C11H12O4 |
| Molar Mass | 208.21 |
ethyl (2S)-2,3-dihydro-1,4-benzodioxine-2-carboxylate - Introduction
Ethyl (2S)-2,3-dihydro-1 is an organic compound with the chemical formula C12H12O4. It is a colorless liquid at room temperature. It is an optically active compound with one chiral center and exists in the (S)-configuration.
Ethyl (2S)-2,3-dihydro-1 has a wide range of applications in pharmaceutical chemistry. It can be used as a raw material for the resolution and synthesis of chiral compounds, and is one of the important intermediates for the synthesis of many drugs. It can also be used as an indirect synthetic reagent for the preparation of biologically active compounds.
there are various methods for synthesizing Ethyl (2S)-2,3-dihydro-1. the common method is to obtain it through the synthesis reaction of benzodioxane, for example, using carbon dioxide and alcohol in the presence of alkaline conditions. The specific preparation method can refer to the relevant literature.
Regarding safety information, due to the lack of specific toxicity data, necessary protective measures need to be taken. Appropriate protective equipment such as lab gloves, goggles and lab coats should be worn during operation. In addition, it should be operated in a well-ventilated place to avoid inhalation and skin contact. Before handling the compound, be sure to read and follow the relevant safety procedures.
Ethyl (2S)-2,3-dihydro-1 has a wide range of applications in pharmaceutical chemistry. It can be used as a raw material for the resolution and synthesis of chiral compounds, and is one of the important intermediates for the synthesis of many drugs. It can also be used as an indirect synthetic reagent for the preparation of biologically active compounds.
there are various methods for synthesizing Ethyl (2S)-2,3-dihydro-1. the common method is to obtain it through the synthesis reaction of benzodioxane, for example, using carbon dioxide and alcohol in the presence of alkaline conditions. The specific preparation method can refer to the relevant literature.
Regarding safety information, due to the lack of specific toxicity data, necessary protective measures need to be taken. Appropriate protective equipment such as lab gloves, goggles and lab coats should be worn during operation. In addition, it should be operated in a well-ventilated place to avoid inhalation and skin contact. Before handling the compound, be sure to read and follow the relevant safety procedures.
Last Update：2024-04-09 20:52:54
