CAS 1193-79-9

2-Acetyl-5-methylfuran

Description:

2-Acetyl-5-methylfuran is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing one oxygen atom. This compound features an acetyl group and a methyl group attached to the furan ring, specifically at the 2 and 5 positions, respectively. It is a colorless to pale yellow liquid with a sweet, caramel-like odor, making it of interest in flavor and fragrance applications. The molecular formula of 2-Acetyl-5-methylfuran indicates it contains carbon, hydrogen, and oxygen atoms, contributing to its reactivity and solubility in organic solvents. It is known for its role in various chemical reactions, including those involving electrophilic aromatic substitution due to the electron-donating nature of the methyl group. Additionally, 2-Acetyl-5-methylfuran can be synthesized through various methods, including the reaction of furan derivatives with acetylating agents. Its properties and reactivity make it a valuable compound in organic synthesis and industrial applications.

Formula: C₇H₈O₂

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

InChI key: InChIKey=KEFJLCGVTHRGAH-UHFFFAOYSA-N

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

Synonyms:

• 1-(5-Methyl-2-furanyl)ethanone
• 1-(5-Methylfuran-2-Yl)Ethanone
• 1-(5-Methylfuran-2-yl)ethan-1-one
• 2-Acetyl-5-methylfural
• 2-Methyl-5-acetylfuran
• 5-Acetyl-2-methylfuran
• 5-Methyl-2-Acetyl Furan
• 5-Methyl-2-Acetylfuran
• 5-Methyl-2-furylethanone
• Ethanone, 1-(5-methyl-2-furanyl)-
• Ketone, methyl 5-methyl-2-furyl

2-Acetyl-5-methylfuran

CAS: 1193-79-9

Formula: C₇H₈O₂

Purity: >98.0%(GC)

Color and Shape: Light yellow to Brown clear liquid

Molecular weight: 124.14

Ref: 3B-A0983

2-Acetyl-5-methylfuran, 98+%

CAS: 1193-79-9

Glucose was transformed to various furan compounds and carboxylic acids derivatives by heat treatment of autoclave such as levulinic acid, 2-acetylfuran and 2-acetyl-5-methylfuran. using 2-acetyl-5-methylfuran or 1,5-dimethyl-2-pyrrolecarbonitrile as reactants, that the formation of the 4-arylation

Formula: C₇H₈O₂

Purity: 98+%

Color and Shape: Liquid, Clear yellow

Molecular weight: 124.14

Ref: 02-A16172

Ethanone, 1-(5-methyl-2-furanyl)-

CAS: 1193-79-9

Formula: C₇H₈O₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 124.1372

Ref: IN-DA000IJS

1-(5-Methylfuran-2-yl)ethanone

CAS: 1193-79-9

1-(5-Methylfuran-2-yl)ethanone exhibits antibacterial activity against Mycobacterium tuberculosis and can be used in related research in the field of life sciences.

Formula: C₇H₈O₂

Purity: 99.94%

Color and Shape: Solid

Molecular weight: 124.14

Ref: TM-TN9363

2-Acetyl-5-methylfuran

CAS: 1193-79-9

2-Acetyl-5-methylfuran

Purity: 98%

Molecular weight: 124.13722g/mol

Ref: 54-OR6003

1-(5-Methylfuran-2-yl)ethanone

CAS: 1193-79-9

Formula: C₇H₈O₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 124.139

Ref: 10-F319334

2-Acetyl-5-methylfuran

CAS: 1193-79-9

Applications 2-Acetyl-5-methylfuran is a useful research chemical and a synthesis intermediate.
References Rong, J., et al.: Org. Lett., 20, 4081 (2018); Zhou, Y., et al.: Chem. Biol. Drug Des., 90, 936 (2017); Smit, F. J., et al.: Med. Chem. Res., 25, 568 (2016)

Formula: C₇H₈O₂

Color and Shape: Neat

Molecular weight: 124.137

Ref: TR-A189008

5-Methyl-2-acetylfuran

CAS: 1193-79-9

5-Methyl-2-acetylfuran is a solid phase microextraction (SPME) sample that is used as an oxidation catalyst. It is a homogeneous catalyst, which means it does not require the presence of any other substances or catalysts. The reaction mechanism of 5-methyl-2-acetylfuran is that the carbonyl group reacts with oxygen to produce an alcohol and aldehyde group. 5-Methyl-2-acetylfuran has been shown to be effective in the synthesis of fatty acids by hydrogenation in flow systems. This process can also be performed using copper complexes.

Purity: Min. 95%

Ref: 3D-FM00813