CAS 13101-45-6

1-(3-Methyl-2-furanyl)ethanone

Description:

1-(3-Methyl-2-furanyl)ethanone, also known by its CAS number 13101-45-6, is an organic compound characterized by its furan ring structure, which contributes to its aromatic properties. This compound features a ketone functional group, specifically an ethanone moiety, attached to a 3-methyl-2-furanyl group. The presence of the furan ring imparts unique reactivity and stability, making it of interest in various chemical applications, including synthesis and flavoring. It is typically a colorless to pale yellow liquid with a distinctive odor, often associated with sweet and fruity notes. The compound is soluble in organic solvents, which enhances its utility in formulations. Its chemical properties include potential reactivity in electrophilic aromatic substitution and nucleophilic addition reactions due to the electron-rich nature of the furan ring. Safety data should be consulted for handling, as with many organic compounds, it may pose health risks if ingested or inhaled. Overall, 1-(3-Methyl-2-furanyl)ethanone is a notable compound in organic chemistry with applications in both industrial and research settings.

Formula: C₇H₈O₂

InChI: InChI=1S/C7H8O2/c1-5-3-4-9-7(5)6(2)8/h3-4H,1-2H3

InChI key: InChIKey=RJBGVAIXGHZIDY-UHFFFAOYSA-N

SMILES: C(C)(=O)C1=C(C)C=CO1

Synonyms:

• Ethanone, 1-(3-methyl-2-furanyl)-
• Ketone, methyl 3-methyl-2-furyl
• 2-Acetyl-3-methylfuran
• 1-(3-Methylfuran-2-yl)ethan-1-one
• 1-(3-Methyl-2-furanyl)ethanone

1-(3-Methylfuran-2-yl)ethanone

CAS: 13101-45-6

Formula: C₇H₈O₂

Molecular weight: 124.1372

Ref: IN-DA000VBV

1-(3-Methylfuran-2-yl)ethan-1-one

CAS: 13101-45-6

1-(3-Methylfuran-2-yl)ethan-1-one is a heterocyclic compound that can be found in the leaves and tubercles of Bignoniaceae plants. It is structurally related to an oxygen heterocycle, which is a class of organic compounds with oxygen in their molecular structures. 1-(3-Methylfuran-2-yl)ethan-1-one has been isolated from the leaves of Blechnum pennaefolium and the tubers of Tuberculosa leontopodioides by alkaline hydrolysis. It has shown antimicrobial activity against Gram positive bacteria. The diacetate form was isolated from the leaves of Bignonia colemanii and shown to have antiviral properties. Formylation reactions are also possible with this compound, as it has been shown to react with sodium methoxide or dimethyl sulfoxide to produce formaldehyde and methanal respectively.

Formula: C₇H₈O₂

Purity: Min. 95%

Molecular weight: 124.14 g/mol

Ref: 3D-NAA10145