CAS 1118786-97-2

5-[(Methylthio)methyl]-2-furancarboxaldehyde

Description:

5-[(Methylthio)methyl]-2-furancarboxaldehyde is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing oxygen. This compound features a carboxaldehyde functional group, indicating the presence of a carbonyl group (C=O) adjacent to a hydrogen atom, which contributes to its reactivity and potential applications in organic synthesis. The methylthio group (-S-CH3) attached to the furan ring enhances its chemical properties, potentially influencing its solubility and reactivity. This compound may exhibit interesting biological activities, making it of interest in fields such as medicinal chemistry and agrochemicals. Its unique structure allows for various synthetic modifications, which can lead to the development of derivatives with tailored properties. Additionally, the presence of both the furan and aldehyde functionalities suggests potential applications in flavor and fragrance industries, as well as in the synthesis of more complex organic molecules. As with many organic compounds, safety data and handling precautions should be considered when working with this substance.

Formula: C₇H₈O₂S

InChI: InChI=1S/C7H8O2S/c1-10-5-7-3-2-6(4-8)9-7/h2-4H,5H2,1H3

InChI key: InChIKey=RSOMHZIAWGSUFR-UHFFFAOYSA-N

SMILES: C(SC)C=1OC(C=O)=CC1

Synonyms:

• 2-Furancarboxaldehyde, 5-[(methylthio)methyl]-
• 5-[(Methylthio)methyl]-2-furancarboxaldehyde

5-[(Methylsulfanyl)methyl]furan-2-carbaldehyde

CAS: 1118786-97-2

5-[(Methylsulfanyl)methyl]furan-2-carbaldehyde is a sulfonated, graphitic carbon with a nitride that can be used as a sustainable and environmentally friendly chemical. It has been shown to have biological and chemical activities at temperatures up to 200°C. 5-[(Methylsulfanyl)methyl]furan-2-carbaldehyde has also been used in the synthesis of carbohydrates for use in biomass applications.

Formula: C₇H₈O₂S

Purity: Min. 95%

Molecular weight: 156.2 g/mol

Ref: 3D-TUB78697