Ethyl 1,3-dithiolane-2-carboxylate is a chemical compound characterized by its unique structure, which includes a dithiolane ring and an ester functional group. This compound typically appears as a colorless to pale yellow liquid and has a distinctive odor. It is soluble in organic solvents, making it useful in various chemical applications. The presence of the dithiolane ring contributes to its reactivity, particularly in nucleophilic substitution reactions and as a potential building block in organic synthesis. Ethyl 1,3-dithiolane-2-carboxylate can also participate in cycloaddition reactions and is of interest in the development of pharmaceuticals and agrochemicals due to its potential biological activity. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if inhaled or ingested. Proper storage in a cool, dry place away from incompatible substances is recommended to maintain its stability and integrity.

Ethyl 1,3-dithiolane-2-carboxylate

20461-99-8: 1,3-Dithiolane-2-Carboxylic Acid, Ethyl Ester, 1,3-Dithiolane-2-carboxylicacid,ethyl ester, 2-Ethoxycarbonyl-1,3-dithiolane, Ethyl 1,3-dithiolane-2-carboxylate

Ethyl 1,3-dithiolane-2-carboxylate is a chiral carbonyl compound that has been used as an intermediate in the synthesis of a variety of organic compounds. The asymmetric synthesis of this compound has been achieved using a desulfurization mediated by tertiary amines and catalytic amounts of copper salts. It has shown receptor activity against aldehydes and anions. This compound also reacts with enolates to form thioacetals, which can be further reacted to give chiral products.

CAS 20461-99-8: Ethyl 1,3-dithiolane-2-carboxylate

Ethyl 1,3-Dithiolane-2-carboxylate

Ref: 3D-FE61235

Ethyl 1,3-dithiolane-2-carboxylate

Ref: 10-F238852

ethyl 1,3-dithiolane-2-carboxylate

Ref: 54-OR30390

1,3-Dithiolane-2-carboxylic acid, ethyl ester

Ref: IN-DA0029LV