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CAS 41908-01-4

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(5-acetyl-3-thienyl)methyl acetate

Description:
(5-acetyl-3-thienyl)methyl acetate is an organic compound characterized by its thienyl ring structure, which is a five-membered aromatic ring containing sulfur. This compound features an acetyl group and a methyl acetate moiety, contributing to its reactivity and potential applications in organic synthesis. The presence of the thienyl group imparts unique electronic properties, making it useful in various chemical reactions, including electrophilic substitutions. The acetyl group enhances the compound's ability to participate in acylation reactions, while the methyl acetate portion provides a functional group that can be hydrolyzed or transformed in further synthetic pathways. This compound may exhibit moderate to low solubility in water, typical of many organic compounds, but is likely soluble in organic solvents such as ethanol or dichloromethane. Its potential applications could span fields such as pharmaceuticals, agrochemicals, or materials science, where thienyl derivatives are often explored for their biological activity or as intermediates in the synthesis of more complex molecules.
Formula:C9H10O3S
InChI:InChI=1/C9H10O3S/c1-6(10)9-3-8(5-13-9)4-12-7(2)11/h3,5H,4H2,1-2H3
SMILES:CC(=O)c1cc(COC(=O)C)cs1
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