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CAS 108499-33-8

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Methyl (2-furanylmethyl)thioacetate

Description:
Methyl (2-furanylmethyl)thioacetate is an organic compound characterized by its unique structure, which includes a furan ring and a thioester functional group. This compound typically appears as a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. The presence of the furan moiety contributes to its potential reactivity, particularly in electrophilic aromatic substitution reactions. Methyl (2-furanylmethyl)thioacetate may exhibit biological activity, making it of interest in fields such as medicinal chemistry and fragrance formulation. Its thioacetate group can undergo hydrolysis to release the corresponding thiol and acetic acid, which may further participate in various chemical reactions. As with many organic compounds, safety precautions should be taken when handling this substance, as it may pose health risks if ingested or inhaled. Overall, its unique structure and properties make it a compound of interest in both synthetic and applied chemistry contexts.
Formula:C8H10O3S
InChI:InChI=1/C8H10O3S/c1-10-8(9)6-12-5-7-3-2-4-11-7/h2-4H,5-6H2,1H3
SMILES:COC(=O)CSCc1ccco1
Synonyms:
  • Methyl [(Furan-2-Ylmethyl)Sulfanyl]Acetate
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