CAS 32766-64-6
:ethyl (2,5-dichlorothiophen-3-yl)(oxo)acetate
Description:
Ethyl (2,5-dichlorothiophen-3-yl)(oxo)acetate, with the CAS number 32766-64-6, is a chemical compound characterized by its unique structure that includes a thiophene ring substituted with two chlorine atoms and an oxoacetate functional group. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, including potential reactivity due to the presence of the electrophilic carbonyl group. The dichlorothiophene moiety may impart specific electronic and steric effects, influencing its reactivity and interactions in various chemical environments. Ethyl (2,5-dichlorothiophen-3-yl)(oxo)acetate may be utilized in organic synthesis and medicinal chemistry, potentially serving as an intermediate in the development of pharmaceuticals or agrochemicals. Its solubility, stability, and reactivity can vary based on the solvent and conditions used, making it important to consider these factors in practical applications. As with many chemical substances, safety data and handling precautions should be reviewed to ensure proper management in laboratory or industrial settings.
Formula:C8H6Cl2O3S
InChI:InChI=1/C8H6Cl2O3S/c1-2-13-8(12)6(11)4-3-5(9)14-7(4)10/h3H,2H2,1H3
SMILES:CCOC(=O)C(=O)c1cc(Cl)sc1Cl
Synonyms:- Ethyl (2,5-Dichlorothien-3-Yl)(Oxo)Acetate
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Found 2 products.
Ethyl 2-(2,5-dichlorothiophen-3-yl)-2-oxoacetate
CAS:<p>This compound is a selective hydrogenation catalyst with a high degree of selectivity for the reduction of chlorinated aliphatic and aromatic compounds. The catalyst can be immobilized on different supports, such as palladium on alumina or carbon. It has been shown that the nature of the support has an effect on the catalytic activity and selectivity. This immobilized catalyst is more stable than unsupported catalysts and it can be used in batch processes.</p>Formula:C8H6Cl2O3SPurity:Min. 95%Molecular weight:253.1 g/mol
